ICLEVIA- levonorgestrel and ethinyl estradiol kit

Iclevia by

Drug Labeling and Warnings

Iclevia by is a Prescription medication manufactured, distributed, or labeled by Aurobindo Pharma Limited. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

  • BOXED WARNING (What is this?)

    WARNING: CIGARETTE SMOKING AND SERIOUS CARDIOVASCULAR EVENTS


    Cigarette smoking increases the risk of serious cardiovascular events from combination oral contraceptive (COC) use. This risk increases with age, particularly in women over 35 years of age, and with the number of cigarettes smoked. For this reason, COCs are contraindicated in women who are over 35 years of age and smoke [see Contraindications (4)].

  • 1 INDICATIONS AND USAGE

    IcleviaTM (levonorgestrel and ethinyl estradiol tablets) is indicated for use by females of reproductive potential to prevent pregnancy.

  • 2 DOSAGE AND ADMINISTRATION

    2.1 How to Start Iclevia

    Iclevia is dispensed in an Extended-Cycle Wallet [see How Supplied/Storage and Handling (16)].  Iclevia should be started on a Sunday (see Table 1). For the first cycle of a Sunday Start regimen, an additional method of contraception should be used until after the first 7 consecutive days of administration.

    Instruct patients to take Iclevia once a day by mouth at the same time every day for 91 days. To achieve maximum contraceptive effectiveness, Iclevia should be taken exactly as directed and at intervals not exceeding 24 hours. For patient instructions regarding missed pills, see FDA-approved patient labeling.

    2.2 How to Take Iclevia



    Table 1:  Instructions for Administration of Iclevia
    Starting COCs in women not currently using hormonal contraception (Sunday Start)
     
     
    Important:
    Consider the possibility of ovulation and conception prior to initiation of this product.
     
     
    Tablet Color:
     
    • Iclevia active tablets are white (Day 1 to Day 84). 
    • Iclevia inactive tablets are green (Day 85 to Day 91).
    		Sunday Start:
    For each 91-day course, take in the following order:
     
    • Take the first white tablet (0.15 mg of levonorgestrel and 0.03 mg  ethinyl estradiol) on the first Sunday after the onset of menstruation. If menstruation begins on a Sunday, take the tablet on that day. Due to the potential risk of becoming pregnant, use additional non-hormonal contraception (such as condoms or spermicide) for the first 7 days of treatment. 
    • Take subsequent white tablets once  daily at the same time each day for a total of 84 days. 
    • Take one green tablet (inert)  daily for the following 7 days and at the same time of day that active tablets were taken. A scheduled period should occur during the 7 days that the green tablets are taken. 
    • Begin the next and all subsequent 91-day   courses of Iclevia without interruption on the same day of the week (i.e., Sunday) on which the patient began her first dose. Follow the same schedule as the initial 91-day course: a white tablet once a day for 84 days, and a green tablet once a day for 7 days. If the patient does not immediately start her next pill pack, instruct her to protect herself from pregnancy by using a non-hormonal back-up method of contraception until she has taken a white tablet daily for 7 consecutive days.
    Switching to Iclevia from another oral contraceptive
    		Start on the same day that a new pack of the previous oral contraceptive would have started.
    Switching from another contraceptive method to Iclevia
    		Start Iclevia:
     
             Transdermal patch
     
    • On the day when the next application would have been scheduled.
     
             Vaginal ring
     
    • On the day when the next insertion would have been scheduled.
     
             Injection
     
    • On the day when the next injection would have been scheduled.
     


             Intrauterine contraceptive (IUD)
     
    • On the day of removal.
    • If the IUD is not removed on first day of the patient’s menstrual cycle, additional non- hormonal contraception (such as condoms or spermicide) is needed for the first seven days of the first 91-day course.
            Implant
    • On the day of removal.
    Complete instructions to facilitate patient counseling on proper tablet usage are located in the FDA-approved patient labeling.

    Starting Iclevia after Abortion or Miscarriage


    First-trimester


    • After a first-trimester abortion or miscarriage, Iclevia may be started immediately. An additional method of contraception is not needed if Iclevia is started immediately.
    • If Iclevia is not started within 5 days after termination of the pregnancy, the patient should use additional non-hormonal contraception (such as condoms or spermicide) for the first seven days of her first 91-day course of Iclevia.

    Second-trimester


    • Do not start until 4 weeks after a second-trimester abortion or miscarriage, due to the increased risk of thromboembolic disease. Start Iclevia following the instructions in  Table 1 for Sunday start. Use additional non-hormonal contraception (such as condoms or spermicide) for the first seven days of the patient’s first 91-day course of Iclevia  [see Contraindications (4), Warnings and Precautions (5.1), and FDA-approved Patient Labeling].

    Starting Iclevia after Childbirth


    Wallet Instructions:


    • The Wallet consists of 3 blister strips that hold 91 individually sealed pills (a 13-week, or 91-day, cycle). The 91 pills consist of 84 white pills (active pills with hormones) and 7 green pills (inactive pills without hormone).
    • The blister strips 1 and 2 each contain 28 white pills (4 rows of 7 pills). See Figure A.

    figure1

    • The blister strip 3 contains 35 pills consisting of 28 white pills (4 rows of 7 pills) and 7 green pills (1 row of 7 pills). See Figure B.

    figure2 



    • Advise the patient to remove the first pill in the upper left corner by pushing down on the pill. The pill will come out through a hole in the back of the Wallet.
    • Advise the patient to wait 24 hours to take the next pill, and continue to take one pill each day until all the pills have been taken.
    • Advise the patient, after taking the last green pill, to start taking the first white pill from a new Wallet the very next day, regardless of when their period started.

    2.3 Missed Tablets


    Table 2: Instructions for Missed Iclevia Tablets
     
    • If one active tablet (white) is missed in Days 1 through 84
    		 
    Take the tablet as soon as possible. Take the next tablet at the regular time and continue taking one tablet a day until the 91-day course is finished.
     
     
     
    • If two consecutive active tablets (white) are missed in Days 1 through 84
    		 
    Take 2 tablets on the day remembered and 2 tablets the next day. Then continue taking one tablet a day until the 91-day course is finished. Additional non-hormonal contraception (such as condoms or spermicide) should be used as back-up if the patient has sex within 7 days after missing 2 tablets.
     
    • If three or more consecutive active tablets (white) are missed in Days 1 through 84
    		 
    Do not take the missed tablets. Continue taking one tablet a day until the 91-day course is finished. Additional non-hormonal contraception (such as condoms or spermicide) must be used as back-up if the patient has sex within 7 days after missing 3 tablets.

    2.4 Advice in Case of Gastrointestinal Disturbances

    In case of severe vomiting or diarrhea, absorption may not be complete and additional contraceptive measures should be taken. If vomiting or diarrhea occurs within 3 to 4 hours after taking a white tablet, handle this as a missed tablet  [see FDA-approved patient labeling].

  • 3 DOSAGE FORMS AND STRENGTHS

    Iclevia (levonorgestrel and ethinyl estradiol tablets USP) are available in Extended-Cycle Wallets, each containing a 13-week supply of tablets in the following order:


    • 84 white tablets, each containing 0.15 mg of levonorgestrel and 0.03 mg ethinyl estradiol; round, biconvex, beveled-edge tablets debossed with “S” on one side and “27” on other side.
    • 7 green inert tablets; round, mottled, biconvex, beveled-edge uncoated tablets, debossed with “S” on one side and “61” on other side of the tablet.
  • 4 CONTRAINDICATIONS

    Do not prescribe Iclevia to women who are known to have the following conditions:


  • 5 WARNINGS AND PRECAUTIONS

    5.1 Thrombotic Disorders and Other Vascular Problems

    • Stop Iclevia if an arterial thrombotic event or venous thromboembolic (VTE) event occurs.
    • Stop Iclevia if there is unexplained loss of vision, proptosis, diplopia, papilledema, or retinal vascular lesions. Evaluate for retinal vein thrombosis immediately.
    • If feasible, stop Iclevia at least 4 weeks before and through 2 weeks after major surgery or other surgeries known to have an elevated risk of VTE as well as during and following prolonged immobilization.
    • Start Iclevia no earlier than 4 weeks after delivery, in women who are not breastfeeding. The risk of postpartum VTE decreases after the third postpartum week, whereas the risk of ovulation increases after the third postpartum week.
    • The use of COCs increases the risk of VTE. However, pregnancy increases the risk of VTE as much or more than the use of COCs. The risk of VTE in women using COCs is 3 to 9 cases per 10,000 woman- years. The risk of VTE is highest during the first year of use of COCs and when restarting hormonal contraception after a break of 4 weeks or longer. The risk of thromboembolic disease due to COCs gradually disappears after use is discontinued.
    • Use of Iclevia provides women with more hormonal exposure on a yearly basis than conventional monthly COCs containing the same strength synthetic estrogens and progestins (an additional 9 weeks of exposure per year). In the clinical trial, one case of pulmonary embolism was reported. Postmarketing adverse reactions of VTE have been reported in women who used Iclevia.
    • Use of COCs also increases the risk of arterial thromboses such as strokes and myocardial infarctions, especially in women with other risk factors for these events. Stroke has been reported in women associated with the use of Iclevia. COCs have been shown to increase both the relative and attributable risks of cerebrovascular events (thrombotic and hemorrhagic strokes). This risk increases with age, particularly in women over 35 years of age who smoke.
    • Use COCs with caution in women with cardiovascular disease risk factors.

    5.2 Liver Disease

    Impaired Liver Function


    Do not use Iclevia in women with liver disease, such as acute viral hepatitis or severe (decompensated) cirrhosis of the liver [see Contraindications (4)]. Acute or chronic disturbances of liver function may necessitate the discontinuation of COC use until markers of liver function return to normal and COC causation has been excluded. Discontinue Iclevia if jaundice develops.


    Liver Tumors


    Iclevia is contraindicated in women with benign and malignant liver tumors [see Contraindications (4)]. Hepatic adenomas are associated with COC use. An estimate of the attributable risk is 3.3 cases/100,000 COC users. Rupture of hepatic adenomas may cause death through intra-abdominal hemorrhage.


    Studies have shown an increased risk of developing hepatocellular carcinoma in long-term (> 8 years) COC users. However, the attributable risk of liver cancers in COC users is less than one case per million users.

    5.3 Risk of Liver Enzyme Elevations with Concomitant Hepatitis C Treatment

    During clinical trials with the Hepatitis C combination drug regimen that contains obmitasvir/paritaprevir/ritonavir, with or without dasabuvir, ALT elevations greater than 5 times the upper limit of normal (ULN), including some cases greater than 20 times the ULN, were significantly more frequent in women using ethinyl estradiol-containing medications, such as COCs. Discontinue Iclevia prior to starting therapy with the combination drug regimen ombitasvir/paritaprevir/ritonavir, with or without dasabuvir [see Contraindications (4)]. Iclevia can be restarted approximately 2 weeks following completion of treatment with the Hepatitis C combination drug regimen.

    5.4 High Blood Pressure

    Iclevia is contraindicated in women with uncontrolled hypertension or hypertension with vascular disease [see Contraindications (4)]. For women with well-controlled hypertension, monitor blood pressure and stop Iclevia if blood pressure rises significantly.


    An increase in blood pressure has been reported in women taking COCs, and this increase is more likely in older women and with extended duration of use. The incidence of hypertension increases with increasing concentration of progestin.

    5.5 Gallbladder Disease

    Studies suggest a small increased relative risk of developing gallbladder disease among COC users. Use of COCs may worsen existing gallbladder disease.


    A past history of COC-related cholestasis predicts an increased risk with subsequent COC use. Women with a history of pregnancy-related cholestasis may be at an increased risk for COC-related cholestasis.

    5.6 Carbohydrate and Lipid Metabolic Effects

    Carefully monitor prediabetic and diabetic women who are taking Iclevia. COCs may decrease glucose tolerance.


    Consider alternative contraception for women with uncontrolled dyslipidemia. A small proportion of women will have adverse lipid changes while on COCs.


    Women with hypertriglyceridemia, or a family history thereof, may be at an increased risk of pancreatitis when using COCs.

    5.7 Headache

    If a woman taking Iclevia develops new headaches that are recurrent, persistent, or severe, evaluate the cause and discontinue Iclevia if indicated.


    Consider discontinuation of Iclevia in the case of increased frequency or severity of migraine during COC use (which may be prodromal of a cerebrovascular event) [see Contraindications (4)].

    5.8 Bleeding Irregularities and Amenorrhea

    Bleeding and/or spotting that occurs at any time while taking the first 84 tablets of each extended-cycle regimen is considered “unscheduled” bleeding/spotting. Bleeding that occurs during the time a woman takes the seven green inert tablets is considered “scheduled” bleeding.


    Unscheduled and Scheduled Bleeding and Spotting


    Unscheduled (breakthrough) bleeding and spotting sometimes occur in patients on COCs, especially during the first 3 months of use. If unscheduled bleeding persists or occurs after previously regular cycles on Iclevia, check for causes such as pregnancy or malignancy. If pathology and pregnancy are excluded, bleeding irregularities may resolve over time or with a change to a different COC.


    Before prescribing Iclevia, advise the woman to weigh the convenience of fewer scheduled menses (4 per year instead of 13 per year) against the inconvenience of increased unscheduled bleeding and/or spotting.


    The clinical trial of the efficacy of Iclevia (91-day cycles) in preventing pregnancy also assessed scheduled and unscheduled bleeding. The participants in the study were composed primarily of women who had used oral contraceptives previously as opposed to new users. Women with a history of breakthrough bleeding/spotting ≥ 10 consecutive days on oral contraceptives were excluded from the study. More Iclevia subjects, compared to subjects on the comparator 28-day cycle regimen, discontinued prematurely for unacceptable bleeding (7.7% [Iclevia] vs. 1.8% [28-day cycle regimen]).


    Unscheduled bleeding and unscheduled spotting decreased over successive 91-day cycles. Table 3 below presents the number of days with unscheduled bleeding and/or spotting for each respective 91-day cycle.

     

    Table 3: Number of Unscheduled Bleeding and/or Spotting Days per 91-day Cycle
    Q1=Quartile 1: 25% of women had ≤ this number of days of unscheduled bleeding/spotting
    Median: 50% of women had ≤ this number of days of unscheduled bleeding/spotting
    Q3=Quartile 3: 75% of women had ≤ this number of days of unscheduled bleeding/spotting
    Cycle (N)
    		Days of Unscheduled Bleeding and/or Spotting per
    84-Day Interval
    		Median Days Per Subject-Month
    Mean
    		Q1
    		Median
    		Q3
      1 (446)
    		  15.1
    		  3.0
    		  12
    		  23.0
    		  3.0
      2 (368)
    		  11.6
    		  2.0
    		  6
    		  17.5
    		  1.5
      3 (309)
    		  10.6
    		  1.0
    		  6
    		  15.0
    		  1.5
      4 (282)
    		  8.8
    		  1.0
    		  4
    		  14.0
    		  1.0

    Table 4 shows the percentages of women with ≥ 7 days and ≥ 20 days of unscheduled spotting and/or bleeding in the Iclevia and the 28-day cycle treatment groups.

    Table 4: Percentage of Subjects with Unscheduled Bleeding and/or Spotting
    Days of unscheduled bleeding and/or spotting
    		Percentage of Subjectsa
    a Based on spotting and/or bleeding on days 1 to 84 of a 91 day cycle in the Iclevia subjects and days 1 to 21 of a 28 day cycle over 4 cycles in the 28-day dosing regimen.
      Iclevia
    		Cycle 1 (N=385)
    		Cycle 4 (N=261)
      ≥ 7 days
    		65%
    		42%
      ≥ 20 days
    		35%
    		15%
      28-day regimen
    		Cycles 1 to 4 (N=194)
    		Cycles 10 to 13 (N=158)
      ≥ 7 days
    		38%
    		39%
      ≥ 20 days
    		6%
    		4%

    Total days of bleeding and/or spotting (scheduled plus unscheduled) were similar over one year of treatment for Iclevia subjects and subjects on the 28-day cycle regimen.


    Amenorrhea and Oligomenorrhea


    Women who are not pregnant and use Iclevia may experience amenorrhea. Based on data from the clinical trial, amenorrhea occurred in approximately 0.8% of women during Cycle 1, 1.2% of women during Cycle 2, 3.7% of women during Cycle 3, and 3.4% of women during Cycle 4. Because women using Iclevia will likely have scheduled bleeding only 4 times per year, rule out pregnancy at the time of any missed menstrual period.


    Some women may experience amenorrhea or oligomenorrhea after stopping COCs, especially when such a condition was pre-existent.

    5.9 COC Use Before or During Early Pregnancy

    Extensive epidemiological studies have revealed no increased risk of birth defects in women who have used oral contraceptives prior to pregnancy. Studies also do not suggest a teratogenic effect, particularly in so far as cardiac anomalies and limb-reduction defects are concerned, when oral contraceptives are taken inadvertently during early pregnancy. Discontinue Iclevia use if pregnancy is confirmed.


    Administration of oral contraceptives to induce withdrawal bleeding should not be used as a test for pregnancy [see Use in Specific Populations (8.1)].

    5.10 Depression

    Depression associated with the use of Iclevia has been reported. Carefully observe women with a history of depression and discontinue Iclevia if severe depression recurs.

    5.11 Carcinoma of the Breast and Cervix

    • Iclevia is contraindicated in women who currently have or have had breast cancer because breast cancer may be hormonally sensitive [see Contraindications (4)].

    There is substantial evidence that COCs do not increase the incidence of breast cancer. Although some past studies have suggested that COCs might increase the incidence of breast cancer, more recent studies have not confirmed such findings.


    • Some studies suggest that COC use has been associated with an increase in the risk of cervical cancer or intraepithelial neoplasia. However, there continues to be controversy about the extent to which such findings may be due to differences in sexual behavior and other factors.

    5.12 Effect on Binding Globulins

    The estrogen component of COCs may raise the serum concentrations of thyroxine-binding globulin, sex hormone-binding globulin and cortisol-binding globulin. The dose of replacement thyroid hormone or cortisol therapy may need to be increased.

    5.13 Monitoring

    A woman who is taking COCs should have a yearly visit with her healthcare provider for a blood pressure check and for other indicated health care.

    5.14 Hereditary Angioedema

    In women with hereditary angioedema, exogenous estrogens may induce or exacerbate symptoms of angioedema.

    5.15 Chloasma

    Chloasma may occasionally occur, especially in women with a history of chloasma gravidarum. Women with a tendency to develop chloasma should avoid prolonged exposure to the sun or ultraviolet radiation while taking Iclevia.

  • 6 ADVERSE REACTIONS

    The following serious adverse reactions with the use of COCs are discussed elsewhere in the labeling:



    Adverse reactions commonly reported by COC users are:


    • Irregular uterine bleeding
    • Nausea
    • Breast tenderness
    • Headache

    6.1 Clinical Trial Experience

    Because clinical trials are conducted under widely varying conditions, adverse reaction rates observed in the clinical trials of a drug cannot be directly compared to the rates in the clinical trials of another drug and may not reflect the rates observed in clinical practice.


    The clinical trial that evaluated the safety and efficacy of Iclevia was a 12-month, randomized, multicenter, open-label study, which enrolled women aged 18 to 40, of whom 456 took at least one dose of Iclevia (345.14 woman-years of exposure) [see Clinical Studies (14)].


    Adverse Reactions Leading to Study Discontinuation: 14.9% of the women discontinued from the clinical trial due to an adverse reaction; the most common adverse reactions (≥ 1% of women) leading to discontinuation in the Iclevia group were menorrhagia (5.7%), mood swings (1.9%), weight/appetite increase (1.5%), and acne (1.3%).


    Common Adverse Reactions (≥ 2% of women): headache (20.6%), menorrhagia (11.6%), nausea (7.5%), dysmenorrhea (5.7%), acne (4.6%), migraine (4.4%), breast tenderness (3.5%), weight increased (3.1%), and depression (2.1%).


    Serious Adverse Reactions: pulmonary embolus, cholecystitis.

    6.2 Postmarketing Experience

    The following adverse reactions have been identified during post-approval use of Iclevia. Because these reactions are reported voluntarily from a population of uncertain size, it is not possible to reliably estimate their frequency or establish a causal relationship to drug exposure.


    Gastrointestinal disorders: abdominal distension, vomiting

    General disorders and administration site conditions: chest pain, fatigue, malaise, edema peripheral, pain

    Immune system disorder: hypersensitivity reactions, including itching, rash, and angioedema

    Investigations: blood pressure increased

    Musculoskeletal and connective tissue disorders: muscle spasms, pain in extremity

    Nervous system disorders: dizziness, loss of consciousness

    Psychiatric disorders: insomnia

    Reproductive and breast disorders: dysmenorrhea

    Skin and subcutaneous tissue disorders: alopecia

    Vascular disorders: thrombosis, pulmonary embolism, pulmonary thrombosis

  • 7 DRUG INTERACTIONS

    Consult the labeling of concurrently used drugs to obtain further information about interactions with hormonal contraceptives or the potential for enzyme alterations.

    7.1 Effects of Other Drugs on Combined Oral Contraceptives

    Substances decreasing the plasma concentrations of COCs and potentially diminishing the efficacy of COCs:


    Drugs or herbal products that induce certain enzymes, including cytochrome P450 3A4 (CYP3A4), may decrease the plasma concentrations of COCs and potentially diminish the effectiveness of COCs or increase breakthrough bleeding. Some drugs or herbal products that may decrease the effectiveness of hormonal contraceptives include phenytoin, barbiturates, carbamazepine, bosentan, felbamate, griseofulvin, oxcarbazepine, rifampicin, topiramate, rifabutin, rufinamide, aprepitant, and products containing St. John’s wort. Interactions between oral contraceptives and other drugs may lead to breakthrough bleeding and/or contraceptive failure. Counsel women to use an alternative method of contraception or a back-up method when enzyme inducers are used with COCs, and to continue back-up contraception for 28 days after discontinuing the enzyme inducer to ensure contraceptive reliability.


    Colesevelam: Colesevelam, a bile acid sequestrant, given together with a COC, has been shown to significantly decrease the AUC of EE. The drug interaction between the contraceptive and colesevelam was decreased when the two drug products were given 4 hours apart.


    Substances increasing the plasma concentrations of COCs:


    Co-administration of atorvastatin or rosuvastatin and certain COCs containing ethinyl estradiol (EE) increase AUC values for EE by approximately 20 to 25%. Ascorbic acid and acetaminophen may increase plasma EE concentrations, possibly by inhibition of conjugation. CYP3A4 inhibitors such as itraconazole, voriconazole, fluconazole, grapefruit juice, or ketoconazole may increase plasma hormone concentrations.


    Human immunodeficiency virus (HIV)/ Hepatitis C virus (HCV) protease inhibitors and non-nucleoside reverse transcriptase inhibitors:


    Significant changes (increase or decrease) in the plasma concentrations of estrogen and/or progestin have been noted in some cases of co-administration with HIV protease inhibitors (decrease [e.g., nelfinavir, ritonavir, darunavir/ritonavir, (fos) amprenavir/ritonavir, lopinavir/ritonavir, and tipranavir/ritonavir] or increase [e.g., indinavir and atazanavir/ritonavir])/HCV protease inhibitors (decrease [e.g., nevirapine] or increase [e.g., etravirine]).

    7.2 Effects of Combined Oral Contraceptives on Other Drugs

    COCs containing EE may inhibit the metabolism of other compounds (e.g., cyclosporine, prednisolone, theophylline, tizanidine, and voriconazole) and increase their plasma concentrations.


    COCs have been shown to decrease plasma concentrations of acetaminophen, clofibric acid, morphine, salicylic acid, temazepam and lamotrigine. Significant decrease in plasma concentration of lamotrigine has been shown, likely due to induction of lamotrigine glucuronidation. This may reduce seizure control; therefore, dosage adjustments of lamotrigine may be necessary.


    Women on thyroid hormone replacement therapy may need increased doses of thyroid hormone because the serum concentration of thyroid-binding globulin increases with use of COCs [see Warnings and Precautions (5.12)].

    7.3 Concomitant Use with Hepatitis C Vaccine (HCV) Combination Therapy-Liver Enzyme Elevation

    Do not co-administer Iclevia with HCV drug combinations containing ombitasvir/paritaprevir/ritonavir, with or without dasabuvir, due to potential for ALT elevations [see Warnings and Precautions (5.3)].

    7.4 Interactions with Laboratory Tests

    The use of contraceptive steroids may influence the results of certain laboratory tests, such as coagulation factors, lipids, glucose tolerance, and binding proteins.

  • 8 USE IN SPECIFIC POPULATIONS

    8.1 Pregnancy

    There is little or no increased risk of birth defects in women who inadvertently use COCs during early pregnancy. Epidemiologic studies and meta-analyses have not found an increased risk of genital or non-genital birth defects (including cardiac anomalies and limb-reduction defects) following exposure to low dose COCs prior to conception or during early pregnancy.

    Do not administer COCs to induce withdrawal bleeding as a test for pregnancy. Do not use COCs during pregnancy to treat threatened or habitual abortion.

    8.3 Nursing Mothers

    Advise the nursing mother to use other forms of contraception, when possible, until she has weaned her child. COCs can reduce milk production in breastfeeding mothers. This is less likely to occur once breastfeeding is well established; however, it can occur at any time in some women. Small amounts of oral contraceptive steroids and/or metabolites are present in breast milk.

    8.4 Pediatric Use

    Safety and efficacy of Iclevia have been established in women of reproductive age. Efficacy is expected to be the same for postpubertal adolescents under the age of 18 as for users 18 years and older. Use of Iclevia before menarche is not indicated.

    8.5 Geriatric Use

    Iclevia has not been studied in postmenopausal women and is not indicated in this population.

    8.6 Hepatic Impairment

    The pharmacokinetics of Iclevia have not been studied in subjects with hepatic impairment. However, steroid hormones may be poorly metabolized in patients with hepatic impairment. Acute or chronic disturbances of liver function may necessitate the discontinuation of COC use until markers of liver function return to normal and COC causation has been excluded [see Contraindications (4) and Warnings and Precautions (5.2)].

    8.7 Renal Impairment

    The pharmacokinetics of Iclevia have not been studied in women with renal impairment.

  • 10 OVERDOSAGE

    There have been no reports of serious ill effects from overdose of oral contraceptives, including ingestion by children. Overdosage may cause withdrawal bleeding in females and nausea.

  • 11 DESCRIPTION

    Iclevia (levonorgestrel and ethinyl estradiol tablets USP) is an extended-cycle combination oral contraceptive consisting of 84 white active tablets each containing 0.15 mg of levonorgestrel USP, a synthetic progestin and 0.03 mg of ethinyl estradiol USP, an estrogen, and 7 green inert tablets (without hormones).

    The structural formulas for the active components are:


    Chemistry



    Levonorgestrel is chemically 18,19-Dinorpregn-4-en-20-yn-3-one, 13-ethyl-17-hydroxy-, (17α)-, (-)-.


    Chemistry

    Ethinyl Estradiol is 19-Norpregna-1,3,5(10)-trien-20-yne-3,17-diol, (17α)-.

    • Each white active tablet contains the following inactive ingredients: croscarmellose sodium, lactose monohydrate, magnesium stearate, microcrystalline cellulose, and povidone.
    • Each green inert tablet contains the following inactive ingredients: anhydrous lactose, croscarmellose sodium, FD&C Blue No.2 Aluminum Lake, ferric oxide yellow, magnesium stearate, microcrystalline cellulose, and povidone.

    USP dissolution test is pending.


  • 12 CLINICAL PHARMACOLOGY

    12.1 Mechanism of Action

    COCs lower the risk of becoming pregnant primarily by suppressing ovulation. Other possible mechanisms may include cervical mucus changes that inhibit sperm penetration and endometrial changes that reduce the likelihood of implantation.

    12.2 Pharmacodynamics

    No specific pharmacodynamic studies were conducted with Iclevia.

    12.3 Pharmacokinetics

    Absorption


    No specific investigation of the absolute bioavailability of Iclevia in humans has been conducted. However, literature indicates that levonorgestrel is rapidly and completely absorbed after oral administration (bioavailability nearly 100%) and is not subject to first-pass metabolism. EE is rapidly and almost completely absorbed from the gastrointestinal tract but, due to first-pass metabolism in gut mucosa and liver, the bioavailability of EE is approximately 43%.


    Following continuous dosing with once-daily administration of Iclevia tablets, plasma concentrations of levonorgestrel and EE reached steady-state within 7 days. The mean plasma pharmacokinetic parameters for Iclevia under fasting conditions in normal healthy women following once-daily administration of one levonorgestrel/EE combination tablet for 10 days are summarized in Table 5.

      

    Table 5:  Mean±SD Pharmacokinetic Parameters Under Fasting Conditions in Healthy Women Following 10 Days Administration of One Tablet of Iclevia (n=44)
    Analyte
    		AUC0-24
    		Cmax
    		C min
    		Cavga
    		Tmax
    a Cavg = AUC0-24/24
    Levonorgestrel
    		54.6 ± 16.5
    ng*hr/mL
    		5.0 ± 1.5 ng/mL
    		1.6 ± 0.5
    ng/mL
    		2.3 ± 0.7
    ng/mL
    		1.4 ± 0.7 hours
    Ethinyl estradiol
    		935.5 ± 346.9 pg*hr/mL
    		106.1 ± 41.2 pg/mL 
    		18.5 ± 9.4 pg/mL
    		38.9 ±  14.4 pg/mL 
    		1.6 ± 0.6 hours 

    Food Effect

    The effect of food on the rate and the extent of levonorgestrel and EE absorption following oral administration of Iclevia has not been evaluated.


    Distribution


    The apparent volume of distribution of levonorgestrel and EE are reported to be approximately 1.8 L/kg and 4.3 L/kg, respectively. Levonorgestrel is about 97.5 to 99% protein-bound, principally to sex hormone binding globulin (SHBG) and, to a lesser extent, serum albumin. EE is about 95 to 97% bound to serum albumin. EE does not bind to SHBG, but induces SHBG synthesis, which leads to decreased levonorgestrel clearance. Following repeated daily dosing of levonorgestrel/EE oral contraceptives, levonorgestrel plasma concentrations accumulate more than predicted based on single-dose pharmacokinetics, due in part, to increased SHBG levels that are induced by EE, and a possible reduction in hepatic metabolic capacity.


    Metabolism


    Following absorption, levonorgestrel is conjugated at the 17β-OH position to form sulfate and to a lesser extent, glucuronide conjugates in plasma. Significant amounts of conjugated and unconjugated 3α,5β-­tetrahydrolevonorgestrel are also present in plasma, along with much smaller amounts of 3α,5α­-tetrahydrolevonorgestrel and 16β-hydroxylevonorgestrel. Levonorgestrel and its phase I metabolites are excreted primarily as glucuronide conjugates. Metabolic clearance rates may differ among individuals by several-fold, and this may account in part for the wide variation observed in levonorgestrel concentrations among users.


    First-pass metabolism of EE involves formation of EE-3-sulfate in the gut wall, followed by 2-hydroxylation of a portion of the remaining untransformed EE by hepatic cytochrome P-450 3A4 (CYP3A4). Levels of CYP3A4 vary widely among individuals and can explain the variation in rates of EE hydroxylation. Hydroxylation at the 4-, 6-, and 16-positions may also occur, although to a much lesser extent than 2-hydroxylation. The various hydroxylated metabolites are subject to further methylation and/or conjugation.


    Excretion


    About 45% of levonorgestrel and its metabolites are excreted in the urine and about 32% are excreted in feces, mostly as glucuronide conjugates. The terminal elimination half-life for levonorgestrel after a single dose of Iclevia was about 30 hours.


    EE is excreted in the urine and feces as glucuronide and sulfate conjugates, and it undergoes enterohepatic recirculation. The terminal elimination half-life of EE after a single dose of Iclevia was found to be about 15 hours.

  • 13 NONCLINICAL TOXICOLOGY

    13.1 Carcinogenesis, Mutagenesis, Impairment of Fertility

    [see Warnings and Precautions (5.2, 5.11) and Use in Specific Populations (8.1)].

  • 14 CLINICAL STUDIES

    In a 12-month, multicenter, randomized, open-label clinical trial, 456 women aged 18 to 40 were studied to assess the safety and efficacy of Iclevia, completing 809 91-day cycles of exposure. The racial demographic of those enrolled was: Caucasian (77%), African-American (11%), Hispanic (7%), Asian (2%), and Other (3%).

    There were no exclusions for body mass index (BMI) or weight. The weight range of those women treated was 84 to 304 pounds, with a mean weight of 157 pounds and a median weight of 147 pounds. Among the women in the trial, 63% were current or recent hormonal contraceptive users, 29% were prior users (who had used hormonal contraceptives in the past but not in the 6 months prior to enrollment), and 8% were new starts.

    The pregnancy rate (Pearl Index [PI]) in the 397 women aged 18 to 35 years was 1.98 pregnancies per 100 women-years of use (95% CI: 0.54 to 5.03), based on 4 pregnancies that occurred after the onset of treatment and within 14 days after the last combination pill. Cycles in which conception did not occur, but which included the use of back-up contraception, were not included in the calculation of the PI.

  • 16 HOW SUPPLIED/STORAGE AND HANDLING

    16.1 How Supplied

    Iclevia (levonorgestrel and ethinyl estradiol tablets USP) are available in Extended-Cycle Wallets, each containing a 13-week supply of tablets in the following order:


    • 84 white tablets, each containing 0.15 mg of levonorgestrel and 0.03 mg ethinyl estradiol; round, biconvex, beveled-edge tablets debossed with “S” on one side and “27” on other side.
    • 7 green inert tablets; round, mottled, biconvex, beveled-edge uncoated tablets, debossed with “S” on one side and “61” on other side of the tablet.

                   Pouch of 1 Extended-Cycle Wallet               NDC 65862- 865-94
                   Carton of 3 Pouches                                   NDC 65862- 865-83

    16.2 Storage Conditions


    • Store at 20º to 25°C (68° to 77º F) [see USP Controlled Room Temperature].
    • Protect from light.
  • 17 PATIENT COUNSELING INFORMATION

    See FDA-approved patient labeling (Patient Information and Instructions for Use).


    Counsel patients on the following information:


    • Cigarette smoking increases the risk of serious cardiovascular events from COC use, and that women who are over 35 years old and smoke should not use COCs [see Boxed Warning].
    • Increased risk of VTE compared to non-users of COCs is greatest after initially starting a COC or restarting (following a 4-week or greater pill-free interval) the same or a different COC [see Warnings and Precautions (5.1)].
    • Iclevia does not protect against HIV-infection (AIDS) and other sexually transmitted infections.
    • Iclevia is not to be used during pregnancy; if pregnancy occurs during use of Iclevia, instruct the patient to stop further use [see Warnings and Precautions (5.9)].
    • Take one tablet daily by mouth at the same time every day. Instruct patients what to do in the event tablets are missed [see Dosage and Administration (2.3)].
    • Use a back-up or alternative method of contraception when enzyme inducers are used with Iclevia [see Drug Interactions (7.1)].
    • COCs may reduce breast milk production; this is less likely to occur if breastfeeding is well established [see Use in Specific Populations (8.3)].
    • Women who start on COCs postpartum, and who have not yet had a period, should use an additional method of contraception until they have taken a white tablet for 7 consecutive days [see Dosage and Administration (2.2)].
    • Amenorrhea may occur. Because women using Iclevia will likely have scheduled bleeding only 4 times per year, rule out pregnancy at the time of any missed menstrual period [see Warnings and Precautions (5.8)].

    Distributed by:
    Aurobindo Pharma USA, Inc.
    279 Princeton-Hightstown Road
    East Windsor, NJ 08520

    Manufactured by:
    Aurobindo Pharma Limited
    Hyderabad-500 038, India

    Revised: 08/2018

  • Patient Information

    IcleviaTM
    [eye kle' vee ah]
    (levonorgestrel and ethinyl estradiol tablets USP)


    What is the most important information I should know about Iclevia?

    Do not use Iclevia if you smoke cigarettes and are over 35 years old. Smoking increases your risk of serious cardiovascular side effects from hormonal birth control pills, including death from heart attack, blood clots or stroke. This risk increases with age and the number of cigarettes you smoke.


    What is Iclevia?

    Iclevia is a birth control pill (oral contraceptive) used by women to prevent pregnancy.


    How does Iclevia work for contraception?

    Your chance of getting pregnant depends on how well you follow the directions for taking your birth control pills. The better you follow the directions, the less chance you have of getting pregnant.


    Based on the results of clinical studies, about 1 to 5 out of 100 women may get pregnant during the first year they use Iclevia.


    The following chart shows the chance of getting pregnant for women who use different methods of birth control. Each box on the chart contains a list of birth control methods that are similar in effectiveness. The most effective methods are at the top of the chart. The box on the bottom of the chart shows the chance of getting pregnant for women who do not use birth control and are trying to get pregnant.


     Figure 3

    Who should not take Iclevia?

    Do not take Iclevia if you:

    • smoke and are over 35 years of age
    • had blood clots in your arms, legs, lungs, or eyes
    • had a problem with your blood that makes it clot more than normal
    • have certain heart valve problems or irregular heart beat
    • had a stroke
    • had a heart attack
    • have high blood pressure that cannot be controlled by medicine
    • have diabetes with kidney, eye, nerve, or blood vessel damage
    • have certain kinds of severe migraine headaches with aura, numbness, weakness or changes in vision, or any migraine headaches if you are over 35 years of age
    • have liver problems, including liver tumors
    • take any Hepatitis C drug combination containing ombitasvir/paritaprevir/ritonavir, with or without dasabuvir. This may increase levels of the liver enzyme “alanine aminotransferase” (ALT) in the blood.
    • have any unexplained vaginal bleeding
    • are pregnant
    • had breast cancer or any cancer that is sensitive to female hormones

    If any of these conditions happen while you are taking Iclevia, stop taking Iclevia right away and talk to your healthcare provider. Use non-hormonal contraception when you stop taking Iclevia.

    What should I tell my healthcare provider before taking Iclevia?

    Tell your healthcare provider if you:

    • are pregnant or think you may be pregnant
    • are depressed now or have been depressed in the past
    • had yellowing of your skin or eyes (jaundice) caused by pregnancy (cholestasis of pregnancy)
    • are breastfeeding or plan to breastfeed. Iclevia may decrease the amount of breast milk you make. A small amount of the hormones in Iclevia may pass into your breast milk. Talk to your healthcare provider about the best birth control method for you while breastfeeding.

    Tell your healthcare provider about all the medicines you take, including prescription and over-the-counter medicines, vitamins and herbal supplements.


    Iclevia may affect the way other medicines work, and other medicines may affect how well Iclevia works.


    Know the medicines you take. Keep a list of them to show your healthcare provider and pharmacist when you get a new medicine.


    How should I take Iclevia?

    Read the Instructions for Use at the end of this Patient Information.

    What are the possible serious side effects of Iclevia?


    • Like pregnancy, Iclevia may cause serious side effects, including blood clots in your lungs, heart attack, or a stroke that may lead to death. Some other examples of serious blood clots include blood clots in the legs or eyes.

    Serious blood clots can happen especially if you smoke, are obese, or are older than 35 years of age. Serious blood clots are more likely to happen when you:


    • first start taking birth control pills
    • restart the same or different birth control pills after not using them for a month or more

    Call your healthcare provider or go to a hospital emergency room right away if you have:


    • leg pain that will not go away
    •  sudden severe shortness of breath
    •  sudden change in vision or blindness
    •  chest pain
    • a sudden, severe headache unlike your usual headaches
    •  weakness or numbness in your arm or leg
    •  trouble speaking

    Other serious side effects include:

    • liver problems, including:
      • rare liver tumors
      • jaundice (cholestasis), especially if you previously had cholestasis of pregnancy. Call your healthcare provider if you have yellowing of your skin or eyes.
    • high blood pressure. You should see your healthcare provider for a yearly check of your blood pressure.
    • gallbladder problems
    • changes in the sugar and fat (cholesterol and triglycerides) levels in your blood
    • new or worsening headaches including migraine headaches
    • irregular or unusual vaginal bleeding and spotting between your menstrual periods, especially during the first 3 months of taking Iclevia.
    • depression
    • possible cancer in your breast and cervix
    • swelling of your skin especially around your mouth, eyes, and in your throat (angioedema). Call your healthcare provider if you have a swollen face, lips, mouth tongue or throat, which may lead to difficulty swallowing or breathing. Your chance of having angioedema is higher is you have a history of angioedema.
    • dark patches of skin around your forehead, nose, cheeks and around your mouth, especially during pregnancy (chloasma). Women who tend to get chloasma should avoid spending a long time in sunlight, tanning booths, and under sun lamps while taking Iclevia. Use sunscreen if you have to be in the sunlight.

    What are the most common side effects of Iclevia?


    • headache (migraine)
    • acne
    •  heavier or longer periods, pain with periods
    •  breast tenderness
    •  nausea
    •  increase in weight

    These are not all the possible side effects of Iclevia. For more information, ask your healthcare provider or pharmacist.


    You may report side effects to the FDA at 1-800-FDA-1088.


    What else should I know about taking Iclevia?

    • If you are scheduled for any lab tests, tell your healthcare provider you are taking Iclevia. Certain blood tests may be affected by Iclevia.
    • Iclevia does not protect against HIV infection (AIDS) and other sexually transmitted infections.

    How should I store Iclevia?

    • Store Iclevia at room temperature between 20º to 25°C (68° to 77º F).
    • Protect from light.

    General information about the safe and effective use of Iclevia.

    Medicines are sometimes prescribed for purposes other than those listed in a Patient Information leaflet. Do not use Iclevia for a condition for which it was not prescribed. Do not give Iclevia to other people, even if they have the same symptoms that you have.


    This Patient Information summarizes the most important information about Iclevia. You can ask your pharmacist or healthcare provider for information about Iclevia that is written for health professionals.


    For more information, call Aurobindo Pharma USA, Inc. at 1-866-850-2876.


    Do birth control pills cause cancer?

    Birth control pills do not seem to cause breast cancer. However, if you have breast cancer now, or have had it in the past, do not use birth control pills because some breast cancers are sensitive to hormones.


    Women who use birth control pills may have a slightly higher chance of getting cervical cancer. However, this may be due to other reasons such as having more sexual partners.


    What if I want to become pregnant?

    You may stop taking the pill whenever you wish. Consider a visit with your healthcare provider for a pre-pregnancy checkup before you stop taking the pill.


    What should I know about my period when taking     Iclevia?

    When you take Iclevia, which has a 91-day extended dosing cycle, you should have 4 scheduled periods a year (bleeding when you are taking the 7 green pills). However, you will probably have more bleeding or spotting between your scheduled periods than if you were using a birth control pill with a 28-day dosing cycle. During the first Iclevia 91-day treatment cycle, about 1 in 3 women may have 20 or more days of unplanned bleeding or spotting. This bleeding or spotting tends to decrease with time. Do not stop taking Iclevia because of this bleeding or spotting. If the spotting continues for more than 7 days in a row or if the bleeding is heavy, call your healthcare provider.


    What are the ingredients in Iclevia?

    Active ingredients: Each white pill contains levonorgestrel and ethinyl estradiol.


    Inactive ingredients:


    White pills: croscarmellose sodium, lactose monohydrate, magnesium stearate, microcrystalline cellulose, and povidone.


    Green pills: anhydrous lactose, croscarmellose sodium, FD &C Blue No.2 Aluminum Lake, ferric oxide yellow, magnesium stearate, microcrystalline cellulose, and povidone.



    Instructions For Use

    IcleviaTM
    [eye kle' vee ah]
    (levonorgestrel and ethinyl estradiol tablets USP)

    Important Information about taking Iclevia

    • Take 1 pill every day at the same time. Take the pills in the order directed on your wallet.
    • Do not skip your pills, even if you do not have sex often. If you miss pills (including starting the pack late) you could get pregnant. The more pills you miss, the more likely you are to get pregnant.
    • If you have trouble remembering to take Iclevia, talk to your healthcare provider.
    • When you first start taking Iclevia, spotting or light bleeding in between your periods may occur. Contact your healthcare provider if this does not go away after a few months.
    • You may feel sick to your stomach (nauseous), especially during the first few months of taking Iclevia. If you feel sick to your stomach, do not stop taking the pill. The problem will usually go away. If your nausea does not go away, call your healthcare provider.
    • Missing pills can also cause spotting or light bleeding, even when you take the missed pills later. On the days you take 2 pills to make up for missed pills (see What should I do if I miss any Iclevia pills? below), you could also feel a little sick to your stomach.
    • It is not uncommon to miss a period. However, if you miss a period and have not taken Iclevia according to directions, or feel like you may be pregnant, call your healthcare provider. If you have a positive pregnancy test, you should stop taking Iclevia.
    • If you have vomiting or diarrhea within 3 to 4 hours of taking a white pill, take another white pill as soon as possible. Continue taking one pill a day until the 91-day course is finished.
    • If you have vomiting or diarrhea for more than 1 day, your birth control pills may not work as well. Use an additional birth control method, like condoms or spermicide, until you check with your healthcare provider.
    • Stop taking Iclevia at least 4 weeks before you have major surgery and do not restart after the surgery without asking your healthcare provider. Be sure to use other forms of contraception (like condoms or spermicide) during this time period.

    Before you start taking Iclevia:


    • Decide what time of day you want to take your pill. It is important to take it at about the same time every day.
    • Look at your Extended-Cycle Wallet. Your Wallet consists of 3 blister strips that hold 91 individually sealed pills (a 13­-week or 91-day cycle). The 91 pills consists of 84 white and 7 green pills. The blister strips 1 and 2 each contain 28 white pills   (4 rows of 7 pills). See Figure A. The blister strip 3 contains 35 pills consisting of 28 white pills (4 rows of 7 pills) and 7 green pills (1 row of 7 pills). See Figure B. 

    figure1


       



    figure2
    • Also find:
    • Where on the first blister strip in the pack to start taking pills (upper left corner) and
    • In what order to take the pills (follow the weeks)
    • Be sure you have ready at all times another kind of birth control (such as condoms or spermicide), to use as a back-up in case you miss pills.

    When should I start taking Iclevia?

    If you start taking Iclevia and you have not used a hormonal birth control method before:

    • Take the first white pill on the Sunday after your period starts, even if you are still bleeding. If your period begins on Sunday, start the first white pill that same day.
    • Use another method of birth control (such as condoms or spermicides) as a back-up method if you have sex anytime from the Sunday you start your first white pill until the next Sunday (first 7 days).

    If you start taking Iclevia and you are switching from another birth control pill:


    • Start your new Iclevia pack on the same day that you would start the next pack of your previous birth control method.
    • Do not continue taking the pills from your previous birth control pack.

    If you start taking Iclevia and previously used a vaginal ring:


    • Start using Iclevia on the day you would have reapplied the next ring.

    If you start taking Iclevia and previously used a transdermal patch:

    • Start using Iclevia on the day you would have started a new cycle (first patch application).

    If you start taking Iclevia and you are switching from a progestin-only method such as an implant or injection:


    • Start taking Iclevia on the day of removal of your implant, or on the day when you would have had your next injection.

    If you start taking Iclevia and you are switching from an intrauterine device or system (IUD or IUS):


    • Start taking Iclevia on the day of removal of your IUD or IUS.
    • You do not need back-up contraception if your IUD or IUS is removed on the first day (Day 1) of your period. If your IUD or IUS is removed on any other day, use non-hormonal back-up contraception such as condoms or spermicide for the first 7 days that you take Iclevia.

    Keep a calendar to track your period: If this is the first time you are taking birth control pills, read, “When should I start taking Iclevia?” above. Follow these instructions for a Sunday Start.


    Instructions for using your Iclevia Extended-Cycle Wallet:

     

    Sunday Start:


    • Take pill 1 on the Sunday after your period starts. To remove your pill from the wallet, press the pill through the hole in the bottom of the wallet. See Figure C.

    figure4


    • If your period starts on a Sunday, take pill “1” that same day.
    • Take 1 pill at about the same time every day until you have taken the last pill in the wallet.
    • After taking the last green pill on Day 91 from the wallet, start taking the first white pill from a new Extended-Cycle Wallet on the very next day (this should be a Sunday). Take the first pill in the new pack whether or not you are having your period.
    • Use non-hormonal back-up contraception such as condoms or spermicide for the first 7 days of the first cycle that you take Iclevia.

    What should I do if I miss any Iclevia pills?

    If you miss 1 white pill, follow these steps:


    • Take it as soon as you remember. Take the next pill at your regular time. This means you may take 2 pills in 1 day.
    • Then continue taking 1 pill every day until you finish the pack.
    • You do not need to use a back-up birth control method if you have sex.

    If you miss 2 white pills in a row, follow these steps:


    • Take 2 pills on the day you remember and 2 pills the next day.
    • Then continue to take 1 pill every day until you finish the pack.
    • You could become pregnant if you have sex in the 7 days after you miss two pills. You must use a non-hormonal birth control method (such as a condom or spermicide) as a back-up if you have sex during the first 7 days after you restart your pills.

    If you miss 3 or more white pills in a row, follow these steps:

    • Do not take the missed pills. Keep taking 1 pill every day until you have completed all of the remaining pills in the pack. For example, if you start taking the pill on Thursday, take the pill under “Thursday” and do not take the missed pills. You may have bleeding during the week following the missed pills.
    • You could become pregnant if you have sex during the days of missed pills or during the first 7 days after restarting your pills. You must use a non-hormonal birth control method (such as a condom or spermicide) as a back-up when you miss pills and for the first 7 days after you restart your pills. If you do not have your period when you are taking the green pills, call your healthcare provider because you may be pregnant.

    If you have any questions or are unsure about the information in this leaflet, call your healthcare provider.


    This Patient Information and Instructions for Use have been approved by the U.S. Food and Drug Administration.

    Distributed by:
    Aurobindo Pharma USA, Inc.
    279 Princeton-Hightstown Road
    East Windsor, NJ 08520


    Manufactured by:
    Aurobindo Pharma Limited
    Hyderabad-500 038, India


    Revised: 08/2018





  • PACKAGE LABEL-PRINCIPAL DISPLAY PANEL - 0.15 mg/0.03 mg (91 Tablets Pouch)

    NDC: 65862-865-94
    IcleviaTM
    (Levonorgestrel and Ethinyl
    Estradiol Tablets USP)
    0.15 mg/0.03 mg
    Rx only                          1 Extended-Cycle Wallet,
                                                       Containing 91 Tablets

    Contains 1 Extended-Cycle Wallet containing 91 tablets: Eighty-four white
    tablets, each containing 0.15 mg levonorgestrel USP with 0.03 mg ethinyl
    estradiol USP, and seven green inert tablets.



    PACKAGE LABEL-PRINCIPAL DISPLAY PANEL - 0.15 mg/0.03 mg (91 Tablets Pouch)


  • PACKAGE LABEL-PRINCIPAL DISPLAY PANEL - 0.15 mg/0.03 mg (91 Tablets Carton)

    NDC: 65862-865-94
    IcleviaTM
    (Levonorgestrel and Ethinyl
    Estradiol Tablets USP)
    0.15 mg/0.03 mg
    Rx only                          3 Extended-Cycle Wallets,
                                           91 Tablets Each

    THIS PRODUCT (LIKE ALL ORAL CONTRACEPTIVES) IS INTENDED TO PREVENT PREGNANCY. IT DOES NOT
    PROTECT AGAINST HIV INFECTION (AIDS) AND OTHER SEXUALLY TRANSMITTED DISEASES.

    Contains 3 Extended-Cycle Wallets, each containing 91 tablets: Eighty-four white
    tablets, each containing 0.15 mg levonorgestrel USP with 0.03 mg ethinyl
    estradiol USP, and seven green inert tablets.



    PACKAGE LABEL-PRINCIPAL DISPLAY PANEL - 0.15 mg/0.03 mg (91 Tablets Carton)



  • INGREDIENTS AND APPEARANCE
    ICLEVIA 
    levonorgestrel and ethinyl estradiol kit
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC: 65862-865
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC: 65862-865-833 in 1 CARTON06/29/2018
    1NDC: 65862-865-941 in 1 POUCH
    11 in 1 BLISTER PACK; Type 0: Not a Combination Product
    Quantity of Parts
    Part #Package QuantityTotal Product Quantity
    Part 1 84 
    Part 2 7 
    Part 1 of 2
    ICLEVIA 
    levonorgestrel and ethinyl estradiol tablet
    Product Information
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    LEVONORGESTREL (UNII: 5W7SIA7YZW) (LEVONORGESTREL - UNII:5W7SIA7YZW) LEVONORGESTREL0.15 mg
    ETHINYL ESTRADIOL (UNII: 423D2T571U) (ETHINYL ESTRADIOL - UNII:423D2T571U) ETHINYL ESTRADIOL0.03 mg
    Inactive Ingredients
    Ingredient NameStrength
    CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)  
    LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)  
    MAGNESIUM STEARATE (UNII: 70097M6I30)  
    MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)  
    POVIDONE K30 (UNII: U725QWY32X)  
    Product Characteristics
    ColorWHITEScoreno score
    ShapeROUND (Biconvex, Beveled Edge) Size6mm
    FlavorImprint Code S;27
    Contains    
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    ANDAANDA20685006/29/2018
    Part 2 of 2
    INERT 
    inert tablet
    Product Information
    Route of AdministrationORAL
    Inactive Ingredients
    Ingredient NameStrength
    ANHYDROUS LACTOSE (UNII: 3SY5LH9PMK)  
    CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)  
    FD&C BLUE NO. 2 (UNII: L06K8R7DQK)  
    FERRIC OXIDE YELLOW (UNII: EX438O2MRT)  
    MAGNESIUM STEARATE (UNII: 70097M6I30)  
    MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)  
    POVIDONE K30 (UNII: U725QWY32X)  
    Product Characteristics
    ColorGREENScoreno score
    ShapeROUND (Mottled, Biconvex, Beveled Edge,) Size6mm
    FlavorImprint Code S;61
    Contains    
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    ANDAANDA20685006/29/2018
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    ANDAANDA20685006/29/2018
    Labeler - Aurobindo Pharma Limited (650082092)
    Establishment
    NameAddressID/FEIBusiness Operations
    Aurobindo Pharma Limited650381903ANALYSIS(65862-865) , MANUFACTURE(65862-865)

    • Trademark Results [Iclevia]

    Mark Image

    Registration | Serial
    Company
    Trademark
    Application Date
    ICLEVIA
    ICLEVIA
    97756974 not registered Live/Pending
    Aurobindo Pharma Ltd
    2023-01-17
    ICLEVIA
    ICLEVIA
    88359350 not registered Live/Pending
    Aurobindo Pharma Ltd
    2019-03-27
    ICLEVIA
    ICLEVIA
    86770745 not registered Dead/Abandoned
    Aurobindo Pharma Ltd
    2015-09-28
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