LOMUSTINE by Carnegie Pharmaceuticals LLC LOMUSTINE capsule

LOMUSTINE by

Drug Labeling and Warnings

LOMUSTINE by is a Prescription medication manufactured, distributed, or labeled by Carnegie Pharmaceuticals LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

  • BOXED WARNING (What is this?)

    WARNING: DELAYED MYELOSUPPRESSION and RISK OF OVERDOSAGE

    DELAYED MYELOSUPPRESSION

    Lomustine Capsules cause myelosuppression including fatal myelosuppression. Myelosuppression is delayed, dose-related, and cumulative; occurring 4 to 6 weeks after drug administration and persisting for 1 to 2 weeks. Thrombocytopenia is generally more severe than leukopenia. Cumulative myelosuppression from Lomustine Capsules is manifested by greater severity and longer duration of cytopenias. Monitor blood counts for at least 6 weeks after each dose. Do not give Lomustine Capsules more frequently than every 6 weeks [see Warnings and Precautions (5.1), Dosage and Administration (2.2, 2.3)].

    RISK OF OVERDOSAGE

    PRESCRIBE, DISPENSE, AND ADMINISTER ONLY ENOUGH CAPSULES FOR ONE DOSE. Fatal toxicity occurs with overdosage of Lomustine Capsules. Both physician and pharmacist should emphasize to the patient that only one dose of Lomustine Capsules is taken every 6 weeks [see Dosage and Administration (2.1), Warnings and Precautions (5.2), Overdosage (10)].

  • 1 INDICATIONS AND USAGE

    1.1 Brain Tumors

    Lomustine Capsules are indicated for the treatment of patients with primary and metastatic brain tumors following appropriate surgical and/or radiotherapeutic procedures.

    1.2 Hodgkin’s Lymphoma

    Lomustine Capsules are indicated as a component of combination chemotherapy for the treatment of patients with Hodgkin’s lymphoma whose disease has progressed following initial chemotherapy.

  • 2 DOSAGE AND ADMINISTRATION

    2.1 Important Prescribing and Dispensing Information

    PRESCRIBE ONLY ONE DOSE FOR EACH TREATMENT CYCLE. DO NOT DISPENSE ENTIRE CONTAINER. Dispense only a sufficient number of capsules for one dose.

    Confirm the total dose prescribed by the physician and the appropriate combination of capsule strengths.

    Dispense only the appropriate number of Lomustine Capsules required for the administration of a single dose.

    The prescribed dose may consist of two or more different strengths and colors of capsules.

    Instruct patients that Lomustine Capsules are taken as a single oral dose and will not be repeated for at least 6 weeks. Taking more than the recommended dose causes toxicities, including fatal outcomes [see Warnings and Precautions (5.2) and Overdosage (10)].

    Lomustine Capsules is a cytotoxic drug. Follow applicable special handling and disposal procedures.1

    To minimize the risk of dermal exposure, always wear impervious gloves when handling bottles containing Lomustine Capsules. Do not break Lomustine Capsules; avoid exposure to broken capsules. If dermal contact occurs, wash areas of skin contact immediately and thoroughly.

    2.2 Recommended Dose

    The recommended dose of Lomustine Capsules in adult and pediatric patients is 130 mg/m2 taken as a single oral dose every 6 weeks. Round doses to the nearest 5 mg. Give as a single oral dose and do not repeat for at least 6 weeks. Reduce dose to 100 mg/m2 every 6 weeks in patients with compromised bone marrow function. Also reduce dose accordingly when using with other myelosuppressive drugs.

    2.3 Dose Modifications

    Perform weekly complete blood counts and withhold each subsequent dose for more than 6 weeks if needed until platelet counts recover to 100,000/mm3 or greater and leukocytes recover to 4000/mm3 or greater [see Warnings and Precautions (5.1)].

    Modify each dose of Lomustine Capsules according to the hematologic response of the preceding dose as described in Table 1:

    Table 1. Dose Modifications for Lomustine Capsules

    Nadir After Prior Dose

    Dose Adjustment

    Leukocytes (/mm3)

    Platelets (/mm3)

    ≥ 4000

    ≥ 100,000

    None

    3000 – 3999

    75,000 – 99,999

    None

    2000 – 2999

    25,000 – 74,999

    Reduce dose by 30%

    < 2000

    < 25,000

    Reduce dose by 50%

  • 3 DOSAGE FORMS AND STRENGTHS

    Lomustine Capsules, USP are available in three strengths, distinguishable by the color of the capsules:

    • 100 mg capsules (light green/light green)
    • 40 mg capsules (light green/bright white)
    • 10 mg capsules (bright white/bright white)
  • 4 CONTRAINDICATIONS

    None.

  • 5 WARNINGS AND PRECAUTIONS

    5.1 Delayed Myelosuppression

    Lomustine Capsules cause myelosuppression that can result in fatal infections and bleeding. Myelosuppression from Lomustine Capsules is delayed, dose-related, and cumulative. It usually occurs 4 to 6 weeks after drug administration and persists for 1 to 2 weeks. Thrombocytopenia is generally more severe than leukopenia. Cumulative myelosuppression from Lomustine Capsules is manifested by greater severity and longer duration of cytopenias.

    Monitor blood counts for at least 6 weeks after each dose. Do not give Lomustine Capsules more frequently than every 6 weeks. Adjust dose based on nadir blood counts from prior dose [see Dosage and Administration (2.3)].

    5.2 Risk of Overdosage

    Fatal toxicity occurs with overdosage of Lomustine Capsules. Dispensing or administering more than one dose can lead to fatal toxicity.

    Prescribe only one dose at a time. Dispense only enough capsules for one dose. Both physician and pharmacist should emphasize to the patient that only one dose of Lomustine Capsules is taken every 6 weeks [see Dosage and Administration (2.1) and Overdosage (10)].

    5.3 Pulmonary Toxicity

    Pulmonary toxicity characterized by pulmonary infiltrates and/or fibrosis occurs with Lomustine Capsules. Patients with a baseline below 70% of the predicted Forced Vital Capacity (FVC) or Carbon Monoxide Diffusing Capacity (DLCO) are at increased risk. The onset of pulmonary toxicity occurs after an interval of 6 months or longer from the start of therapy, with cumulative doses of Lomustine Capsules usually greater than 1100 mg/m2.

    Obtain baseline pulmonary function tests prior to initiating treatment and repeat frequently during treatment. Permanently discontinue Lomustine Capsules in patients diagnosed with pulmonary fibrosis.

    5.4 Secondary Malignancies

    Secondary malignancies, including acute leukemia and myelodysplasia, occur with long term use.

    5.5 Hepatotoxicity

    Hepatic toxicity, manifested by increased levels of transaminases, alkaline phosphatase, and bilirubin occurs with Lomustine Capsules.

    Monitor liver function.

    5.6 Nephrotoxicity

    Progressive renal failure with a decrease in kidney size occurs with Lomustine Capsules.

    Monitor renal function.

    5.7 Embryo-Fetal Toxicity

    Based on animal data and its mechanism of action, Lomustine Capsules can cause fetal harm when administered to a pregnant woman. Embryo-fetal toxicity and teratogenicity occurred in rats and rabbits receiving lomustine daily during organogenesis at doses approximately two to four times the total human dose of 130 mg/m2 over 6 weeks (0.18 to 0.27 times the single human dose of 130 mg/m2) based on body surface area (BSA). Advise pregnant women of the potential risk to a fetus. Advise females of reproductive potential to use effective contraception during treatment with Lomustine Capsules and for 2 weeks after the final dose. Advise males with female partners of reproductive potential to use effective contraception during treatment with Lomustine Capsules and for 3.5 months after the final dose [see Use in Specific Populations (8.1, 8.3)].

  • 6 ADVERSE REACTIONS

    The following serious adverse reactions are discussed in greater detail in other sections of the labeling:

    The following adverse reactions associated with the use of Lomustine Capsules were identified in clinical trials or postmarketing reports. Because these reactions were reported from a population of uncertain size, it is not possible to estimate their frequency, reliability, or establish a causal relationship to drug exposure.

    Gastrointestinal disorders: nausea, vomiting, and stomatitis

    Ocular disorders: optic atrophy, visual disturbances, and blindness

    Neurologic disorders: disorientation, lethargy, ataxia, and dysarthria

    Other: alopecia

  • 8 USE IN SPECIFIC POPULATIONS

    8.1 Pregnancy

    Risk Summary

    Based on animal data and its mechanism of action, Lomustine Capsules can cause fetal harm when administered to a pregnant woman [see Clinical Pharmacology (12.1)]. There are no available data on Lomustine Capsules exposure in pregnant women. Lomustine was teratogenic in rats and embryotoxic in rabbits at total dose levels approximately two to four times the total human dose of 130 mg/m2 over 6 weeks (0.18 to 0.27 times the single human dose of 130 mg/m2) based on BSA [see Data]. Advise pregnant women of the potential risk to a fetus.

    In the U.S. general population, the estimated background risk of major birth defects and miscarriage in clinically recognized pregnancies is 2-4% and 15-20%, respectively.

    Data

    Animal Data

    Lomustine was administered by intraperitoneal injection daily to pregnant rats during the period of organogenesis at dose levels of 0, 2, 4, 6, and 8 mg/kg. Resorption rates and post-implantation loss occurred at doses greater than or equal to 4 mg/kg (approximately 0.18 times the clinical dose of 130 mg/m2 based on BSA or approximately twice the total clinical dose of lomustine over 6 weeks). Malformations (omphalocele, ectopia cordis, scoliosis, syndactyly, hydrocephalus, microphthalmia, anophthalmia, anomalies of aortic arch, dextrocardia, malpositioning of the ovaries and testes, sternoschisis, and shortened/misshapen bone of the fore or hind limbs) and decreased fetal body weight occurred at all dose levels. In pregnant rabbits treated with lomustine at 3 mg/kg (approximately 0.27 times the 130 mg/m2 clinical dose based on BSA or approximately four times the total clinical dose of lomustine over 6 weeks) during organogenesis, there were increases in abortions and decreases in surviving pup weight that persisted postnatally.

    8.2 Lactation

    Risk Summary

    There is no information on the presence of lomustine or its metabolites in human milk, its effects on the breastfed infant, or its effects on milk production. Because of the potential for serious adverse reactions in breastfed infants from Lomustine Capsules, advise women not to breastfeed during treatment with Lomustine Capsules and for 2 weeks after the final dose.

    8.3 Females and Males of Reproductive Potential

    Contraception

    Females

    Based on animal data and its mechanism of action, Lomustine Capsules can cause fetal harm [see Use in Specific Populations (8.1)]. Advise females of reproductive potential to use effective contraception during treatment and for 2 weeks after the final dose.

    Males

    Based on Lomustine Capsules's mechanism of action, advise males with female partners of reproductive potential to use effective contraception during treatment with Lomustine Capsules and for 3.5 months after the final dose [see Clinical Pharmacology (12.1)].

    Infertility

    Based on animal findings and its mechanism of action, Lomustine Capsules may result in reduced fertility in males and females of reproductive potential [see Nonclinical Toxicology (13.1)].

    8.4 Pediatric Use

    Pediatric use, including dose, is not based on adequate and well-controlled clinical studies.

    8.5 Geriatric Use

    No data in the clinical studies of Lomustine Capsules are available for patients 65 years of age and over to determine whether they respond differently than younger patients. Other reported clinical experience has not identified differences in responses between elderly and younger patients. In general, dose selection for an elderly patient should be cautious, reflecting the greater frequency of decreased hepatic, renal, or cardiac function and of concomitant disease or other drug therapy.

    Lomustine and its metabolites are known to be substantially excreted by the kidney, and the risk of toxic reactions to this drug may be greater in patients with impaired renal function. Because elderly patients are more likely to have decreased renal function, care should be taken in dose selection, and renal function should be monitored.

  • 10 OVERDOSAGE

    Overdosage with Lomustine Capsules has occurred, including fatal cases [see Dosage and Administration (2.1), Warnings and Precautions (5.2)]. Overdosage causes severe myelosuppression, as well as abdominal pain, diarrhea, vomiting, anorexia, lethargy, dizziness, abnormal hepatic function, cough, and shortness of breath.

    No antidotes exist for Lomustine Capsules overdosage.

  • 11 DESCRIPTION

    Lomustine Capsules, USP (lomustine) is an alkylating drug for oral administration. The chemical name for lomustine is 1-(2-chloro-ethyl)-3-cyclohexyl-1-nitrosourea and the molecular formula is C9H16ClN3O2. The molecular weight is 233.71. Lomustine is a yellow powder, which is soluble in 10% ethanol (0.05 mg per mL) and in absolute alcohol (70 mg per mL). Lomustine is insoluble in water (<0.05 mg per mL).

    The chemical structure is:

    image description

    Lomustine Capsules, USP are supplied as 10 mg, 40 mg, and 100 mg capsules and contain the following inactive ingredients: magnesium stearate NF and mannitol USP. The 10 mg capsule shells are composed of gelatin and titanium dioxide. The 40 mg and 100 mg capsule shells are composed of FD&C blue #1, gelatin, iron oxide black, iron oxide yellow, and titanium dioxide. The capsules are printed with black ink composed of iron oxide black, potassium hydroxide, propylene glycol, shellac, and strong ammonia solution.

    FDA approved dissolution method is not listed in the USP Monograph for Lomustine Capsules, USP, 10 mg, 40 mg, and 100 mg.

  • 12 CLINICAL PHARMACOLOGY

    12.1 Mechanism of Action

    Lomustine alkylates DNA and RNA. As with other nitrosoureas, it may also inhibit several key enzymatic processes by carbamoylation of amino acids in proteins.

    12.2 Pharmacodynamics

    The pharmacodynamics of lomustine are unknown.

    12.3 Pharmacokinetics

    Distribution

    Lomustine crosses the blood-brain barrier.

    Elimination

    The serum half-life of lomustine metabolites ranges from 16 hours to 48 hours.

    Metabolism

    Metabolic pathways involved in the elimination of lomustine have not been characterized.

    Excretion

    Following oral administration of radioactive lomustine at doses ranging from 30 mg/m2 to 100 mg/m2, approximately half of the radioactivity administered was excreted in the urine in the form of degradation products within 24 hours.

    Specific Populations

    The impact of patient specific (e.g., age, sex, and race) or disease (e.g., renal or hepatic impairment) characteristics on the pharmacokinetics of lomustine is unknown.

  • 13 NONCLINICAL TOXICOLOGY

    13.1 Carcinogenesis, Mutagenesis, Impairment of Fertility

    Lomustine is carcinogenic in rats and mice, producing a marked increase in tumor incidence in doses lower than those employed clinically.

    In female rats, daily intraperitoneal treatment with lomustine for 2 weeks prior to mating with untreated males resulted in dose dependent decreases in number of corpora lutea and resorption rates with no live births at a dose of 3 mg/kg (approximately 0.14 times the recommended clinical dose of 130 mg/m2 based on body surface area (BSA), or approximately twice the total clinical dose of lomustine over 6 weeks) and decreased pup survival during the first 4 postnatal days at doses greater than or equal to 1.5 mg/kg (a daily dose of approximately 0.06 times the recommended clinical dose of 130 mg/m2 based on BSA or approximately equal to the total clinical dose of lomustine over 6 weeks). Lomustine Capsules may also result in decreased male fertility. Intraperitoneal injection of lomustine resulted in decreased fertility in male rats mated to untreated females based on decreased implantations and decreased fetal body weight at weekly doses greater than or equal to 5 mg/kg (approximately 0.23 times the single clinical dose of 130 mg/m2 based on BSA, or approximately equal to the total clinical dose of lomustine over 6 weeks), and increased resorptions at doses greater than or equal to 2.5 mg/kg/week.

  • 15 REFERENCES

    OSHA. http://www.osha.gov/SLTC/hazardousdrugs/index.html.

  • 16 HOW SUPPLIED/STORAGE AND HANDLING

    16.1 How Supplied

    Lomustine Capsules, USP are available in three strengths, distinguishable by the color of the capsules, in individual bottles of 5 capsules each:

    Strength

    Capsule Description

    NDC Code

    100 mg

    Hard gelatin capsule shell with light green opaque body and light green opaque cap, imprinted with black ink “CP116” on cap, containing white powder.

    80005-116-02

    40 mg

    Hard gelatin capsule shell with light green opaque body and bright white opaque cap, imprinted with black ink “CP115” on cap, containing white powder.

    80005-115-02

    10 mg

    Hard gelatin capsule shell with bright white opaque body and bright white opaque cap, imprinted with black ink “CP114” on cap, containing white powder.

    80005-114-02

    16.2 Storage and Handling

    Store at 20º to 25ºC (68º to 77ºF); excursions permitted to 15° to 30°C (59° to 86°F) [See USP Controlled Room Temperature]. Avoid temperatures over 40°C (104°F).

    Lomustine Capsules, USP is a cytotoxic drug. Follow applicable special handling and disposal procedures.1

    To minimize the risk of dermal exposure, always wear impervious gloves when handling bottles containing Lomustine Capsules, USP. Do not break Lomustine Capsules, USP; avoid exposure to broken capsules. If dermal contact occurs, wash areas of skin contact immediately and thoroughly.

  • 17 PATIENT COUNSELING INFORMATION

    Myelosuppression

    Advise patients that periodic assessment of their blood counts are required. Advise patients to contact their healthcare provider for new onset of bleeding or fever or symptoms of infection [see Warnings and Precautions (5.1)].

    Overdosage

    Advise patients that toxicity including fatal toxicity occurs with Lomustine Capsules overdosage [see Warnings and Precautions (5.2), Overdosage (10), Dosage and Administration (2.1)].

    Advise patients to take Lomustine Capsules as directed:

    • Lomustine Capsules are taken as a single oral dose that will not be repeated for at least 6 weeks.
    • Use of the recommended dose at less than 6 week intervals leads to toxicities including fatal toxicities.
    • Each dose may consist of 2 or more different strengths and colors of capsules.

    Pulmonary Fibrosis

    Advise patients to contact their healthcare provider for new or worsening cough, chest pain, or shortness of breath [see Warnings and Precautions (5.3)].

    Hepatotoxicity

    Inform patients that Lomustine Capsules can cause hepatotoxicity and that liver function monitoring during treatment is necessary [see Warnings and Precautions (5.5)].

    Nephrotoxicity

    Inform patients that Lomustine Capsules can cause nephrotoxicity and that renal function and electrolyte monitoring during treatment is necessary [see Warnings and Precautions (5.6)].

    Embryo-Fetal Toxicity

    Advise females of reproductive potential of the potential risk to a fetus and to inform their healthcare provider of a known or suspected pregnancy [see Warnings and Precautions (5.7), Use in Specific Populations (8.1)].

    Advise females of reproductive potential to use effective contraception during treatment with Lomustine Capsules and for at least 2 weeks after the final dose [see Use in Specific Populations (8.3)].

    Advise male patients with female partners of reproductive potential to use condoms during treatment with Lomustine Capsules and for 4 months after the final dose [see Use in Specific Populations (8.3)].

    Lactation

    Advise women not to breastfeed during treatment with Lomustine Capsules and for 2 weeks after the final dose [see Use in Specific Populations (8.2)].

    Infertility

    Advise females and males of reproductive potential of the potential for reduced fertility from Lomustine Capsules [see Use in Specific Populations (8.3) and Nonclinical Toxicology (13.1)].

    Distributed by:

    Carnegie Pharmaceuticals LLC

    Delran, NJ 08075, USA

    Revised: 07/2025

  • PACKAGE LABEL PRINCIPAL DISPLAY PANEL 

    NDC 80005-114-02
    Lomustine Capsules, USP

    10 mg per capsule

    Caution: DO NOT DISPENSE ENTIRE CONTAINER. Dispense only enough capsules for one dose.

    Rx only
    5 capsules

    Label

    label

    Carton

    carton

    NDC 80005-115-02
    Lomustine Capsules, USP

    40 mg per capsule

    Caution: DO NOT DISPENSE ENTIRE CONTAINER. Dispense only enough capsules for one dose.

    Rx only
    5 capsules
    Label

    label

    Carton

    carton

    NDC 80005-116-02
    Lomustine Capsules, USP

    100 mg per capsule

    Caution: DO NOT DISPENSE ENTIRE CONTAINER. Dispense only enough capsules for one dose.

    Rx only
    5 capsules
    Label

    label

    Carton

    carton

  • INGREDIENTS AND APPEARANCE
    LOMUSTINE 
    lomustine capsule
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC: 80005-114
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    LOMUSTINE (UNII: 7BRF0Z81KG) (LOMUSTINE - UNII:7BRF0Z81KG) LOMUSTINE10 mg
    Inactive Ingredients
    Ingredient NameStrength
    MAGNESIUM STEARATE (UNII: 70097M6I30)  
    MANNITOL (UNII: 3OWL53L36A)  
    GELATIN (UNII: 2G86QN327L)  
    POTASSIUM HYDROXIDE (UNII: WZH3C48M4T)  
    AMMONIA (UNII: 5138Q19F1X)  
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    FERROSOFERRIC OXIDE (UNII: XM0M87F357)  
    SHELLAC (UNII: 46N107B71O)  
    Product Characteristics
    ColorWHITE (bright white opaque body) , white (bright white opaque cap) Scoreno score
    ShapecapsuleSize16mm
    FlavorImprint Code CP;114
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC: 80005-114-025 in 1 BOTTLE; Type 0: Not a Combination Product11/10/2025
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    ANDAANDA21926511/10/2025
    LOMUSTINE 
    lomustine capsule
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC: 80005-115
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    LOMUSTINE (UNII: 7BRF0Z81KG) (LOMUSTINE - UNII:7BRF0Z81KG) LOMUSTINE40 mg
    Inactive Ingredients
    Ingredient NameStrength
    MAGNESIUM STEARATE (UNII: 70097M6I30)  
    MANNITOL (UNII: 3OWL53L36A)  
    GELATIN (UNII: 2G86QN327L)  
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    FERROSOFERRIC OXIDE (UNII: XM0M87F357)  
    FERRIC OXIDE YELLOW (UNII: EX438O2MRT)  
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
    AMMONIA (UNII: 5138Q19F1X)  
    POTASSIUM HYDROXIDE (UNII: WZH3C48M4T)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    SHELLAC (UNII: 46N107B71O)  
    Product Characteristics
    Colorgreen (light green opaque body) , white (bright white opaque cap) Scoreno score
    ShapecapsuleSize18mm
    FlavorImprint Code CP;115
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC: 80005-115-025 in 1 BOTTLE; Type 0: Not a Combination Product11/10/2025
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    ANDAANDA21926511/10/2025
    LOMUSTINE 
    lomustine capsule
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC: 80005-116
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    LOMUSTINE (UNII: 7BRF0Z81KG) (LOMUSTINE - UNII:7BRF0Z81KG) LOMUSTINE100 mg
    Inactive Ingredients
    Ingredient NameStrength
    MAGNESIUM STEARATE (UNII: 70097M6I30)  
    MANNITOL (UNII: 3OWL53L36A)  
    GELATIN (UNII: 2G86QN327L)  
    AMMONIA (UNII: 5138Q19F1X)  
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    FERROSOFERRIC OXIDE (UNII: XM0M87F357)  
    FERRIC OXIDE YELLOW (UNII: EX438O2MRT)  
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
    POTASSIUM HYDROXIDE (UNII: WZH3C48M4T)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    SHELLAC (UNII: 46N107B71O)  
    Product Characteristics
    Colorgreen (light green opaque body) , green (light green opaque cap) Scoreno score
    ShapecapsuleSize19mm
    FlavorImprint Code CP;116
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC: 80005-116-025 in 1 BOTTLE; Type 0: Not a Combination Product11/10/2025
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    ANDAANDA21926511/10/2025
    Labeler - Carnegie Pharmaceuticals LLC (079839141)
    Registrant - Carnegie Pharmaceuticals LLC (079839141)
    Establishment
    NameAddressID/FEIBusiness Operations
    Carnegie Pharmaceuticals LLC079839141manufacture(80005-114, 80005-115, 80005-116)
    • © 2025 FDA.report
    This site is not affiliated with or endorsed by the FDA.