Application 213390

Type
ANDA
Sponsor
NAVISCI

Application Products#

Product, Drug, Ingredient table
ProductDrugIngredientFormStrengthReference drugReference standard
001VIGABATRINVIGABATRINFOR SOLUTION;ORAL500MG/PACKETNoNo

Orange Book products#

Application-product, Trade name, Ingredient table
Application-productTrade nameIngredientStrengthDosage form / routeTE codesRLD / RSApproval date
A213390-001VIGABATRINVIGABATRIN500MG/PACKETFOR SOLUTION / ORAL2021-07-29

openFDA label cross-check#

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Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
VigabatrinVIGABATRINNovadoz Pharmaceuticals LLC082d818a-4f4e-4675-98c6-91db0294e63c2026-06-15Boxed warning, Warnings, Adverse reactionsName fallback
vigabatrinVIGABATRINCarnegie Pharmaceuticals LLC8406bd5a-8887-4579-a11e-5ab449c589632026-02-17Boxed warning, Warnings, Adverse reactionsName fallback
VIGABATRINVIGABATRINPar Health USA, LLCe7cbc0a5-8c28-4451-9176-b608e228ba662026-01-20Boxed warning, Warnings, Adverse reactionsName fallback
vigabatrinVIGABATRINZydus Lifesciences Limitedcd5ebc7a-8d5b-46b4-ad9b-e4a25fa3e26c2025-11-07Boxed warning, Warnings, Adverse reactionsName fallback
vigabatrinVIGABATRINZydus Lifesciences Limitede9c99000-fc0c-4083-b620-ba9ac821f8ac2025-11-07Boxed warning, Warnings, Adverse reactionsName fallback
VigabatrinVIGABATRINAurobindo Pharma Limitedc97ce40c-1c5a-479d-9188-5ce03cf7e0652025-07-15Boxed warning, Warnings, Adverse reactionsName fallback
VigabatrinVIGABATRINActavis Pharma, Inc.8dc7bd15-2636-4d58-b651-dd117ca43dbd2024-09-30Boxed warning, Warnings, Adverse reactionsName fallback
VigabatrinVIGABATRINDr. Reddys Laboratories Inc.,f6be436e-46c7-e9ab-0fcf-e8d04dc12b722024-06-07Boxed warning, Warnings, Adverse reactionsName fallback
vigabatrinVIGABATRINZydus Pharmaceuticals (USA) Inc.6d3fc853-1b2d-47ad-a4f2-f11505601bc22024-03-27Boxed warning, Warnings, Adverse reactionsName fallback
vigabatrinVIGABATRINZydus Pharmaceuticals (USA) Inc.6c0bf4fb-b234-4053-9163-1e8d0142d7182024-03-21Boxed warning, Warnings, Adverse reactionsName fallback
VigabatrinVIGABATRINAurobindo Pharma Limited4aaea88b-e0fd-45e3-bb02-604bf8ee9b5b2024-01-19Boxed warning, Warnings, Adverse reactionsName fallback
VigabatrinVIGABATRINAmneal Pharmaceuticals NY LLC9791494f-492b-487a-8211-7747fb57923e2023-02-28Boxed warning, Warnings, Adverse reactionsName fallback
VigabatrinVIGABATRINAmneal Pharmaceuticals NY LLC5b8fb137-848b-45fd-9107-a6db5a6753602022-12-23Boxed warning, Warnings, Adverse reactionsName fallback
VigabatrinVIGABATRINAmneal Pharmaceuticals NY LLC04fef2ec-c275-405d-91b1-99a74ee8caa22022-11-30Boxed warning, Warnings, Adverse reactionsName fallback
VIGABATRINVIGABATRINAscend Laboratories, LLCee835fb6-2b2b-40c4-b6d7-0ad0e790cda82022-11-16Boxed warning, Warnings, Adverse reactionsName fallback
VigabatrinVIGABATRINEdenbridge Pharmaceuticals LLC.93ba3894-fd97-4432-9f2d-e7050371e91f2022-08-25Boxed warning, Warnings, Adverse reactionsName fallback
VigabatrinVIGABATRINHikma Pharmaceuticals USA Inc5ed8d293-b7d8-4c66-9c31-8075e6f990922022-08-11Boxed warning, Warnings, Adverse reactionsName fallback
VIGABATRINVIGABATRINCipla USA, Inc.823cc915-0350-4780-85ed-cd1c338e429d2022-05-10Boxed warning, Warnings, Adverse reactionsName fallback
VigabatrinVIGABATRINDr. Reddys Laboratories Inc.,0afdc84c-f8ec-330a-31c9-fac4ed2569312020-03-17Boxed warning, Warnings, Adverse reactionsName fallback

Boxed warning cross-check#

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boxed warning

WARNING: PERMANENT VISION LOSS Vigabatrin can cause permanent bilateral concentric visual field constriction, including tunnel vision that can result in disability. In some cases, vigabatrin also can damage the central retina and may decrease visual acuity [see Warnings and Precautions (5.1) ] . The onset of vision loss from vigabatrin is unpredictable, and can occur within weeks of starting treatment or sooner, or at any time after starting treatment, even after months or years. Symptoms of vision loss from vigabatrin are unlikely to be recognized by patients or caregivers before vision loss is severe. Vision loss of milder severity, while often unrecognized by the patient or caregiver, can still adversely affect function. The risk of vision loss increases with increasing dose and cumulative exposure, but there is no dose or exposure known to be free of risk of vision loss. Vision assessment is recommended at baseline (no later than 4 weeks after starting vigabatrin), at least every 3 months during therapy, and about 3 to 6 months after the discontinuation of therapy. Once detected, vision loss due to vigabatrin is not reversible. It is expected that, even with frequent monitoring, some patients will develop severe vision loss. Consider drug discontinuation, balancing benefit and risk, if vision loss is documented. Risk of new or worsening vision loss continues as long as vigabatrin is used. It is possible that vision loss can worsen despite discontinuation of vigabatrin. Because of the risk of vision loss, vigabatrin should be withdrawn from patients with refractory complex partial seizures who fail to show substantial clinical benefit within 3 months of initiation and within 2 to 4 weeks of initiation for patients with infantile spasms, or sooner if treatment failure becomes obvious. Patient response to and continued need for vigabatrin should be periodically reassessed. Vigabatrin should not be used in patients with, or at high risk of, other types of irreversible vision loss unless the benefits of treatment clearly outweigh the risks. Vigabatrin should not be used with other drugs associated with serious adverse ophthalmic effects such as retinopathy or glaucoma unless the benefits clearly outweigh the risks. Use the lowest dosage and shortest exposure to vigabatrin consistent with clinical objectives [see Dosage and Administration (2.1) ] . Because ...

Warnings cross-check#

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warnings and cautions

5 WARNINGS AND PRECAUTIONS Abnormal MRI signal changes and intramyelinic edema have been reported in some infants with Infantile Spasms receiving vigabatrin (5.3 , 5.4) Suicidal behavior and ideation: Antiepileptic drugs, including vigabatrin, increase the risk of suicidal thoughts and behavior (5.5) Withdrawal of AEDs: Taper dose to avoid withdrawal seizures (5.6) Anemia: Monitor for symptoms of anemia (5.7) Somnolence and fatigue: Advise patients not to drive or operate machinery until they have gained sufficient experience on vigabatrin (5.8) 5.1 Permanent Vision Loss Vigabatrin can cause permanent vision loss. Because of this risk and because, when it is effective, vigabatrin provides an observable symptomatic benefit; patient response and continued need for treatment should be periodically assessed. Based upon adult studies, 30 percent or more of patients can be affected with bilateral concentric visual field constriction ranging in severity from mild to severe. Severe cases may be characterized by tunnel vision to within 10 degrees of visual fixation, which can result in disability. In some cases, vigabatrin also can damage the central retina and may decrease visual acuity. Symptoms of vision loss from vigabatrin are unlikely to be recognized by patients or caregivers before vision loss is severe. Vision loss of milder severity, while often unrecognized by the patient or caregiver, can still adversely affect function. Because assessing vision may be difficult in infants and children, the frequency and extent of vision loss is poorly characterized in these patients. For this reason, the understanding of the risk is primarily based on the adult experience. The possibility that vision loss from vigabatrin may be more common, more severe, or have more severe functional consequences in infants and children than in adults cannot be excluded. The onset of vision loss from vigabatrin is unpredictable and can occur within weeks of starting treatment or sooner, or at any time after starting treatment, even after months or years. The risk of vision loss increases with increasing dose and cumulative exposure, but there is no dose or exposure known to be free of risk of vision loss. In patients with refractory complex partial seizures, vigabatrin should be withdrawn if a substantial clinical benefit is not observed within 3 months of initiating treatment. If, in...

warnings and cautions table

Indication Placebo Patients with Events per 1,000 Patients Drug Patients with Events per 1,000 Patients Relative Risk: Incidence of Drug Events in Drug Patients/Incidence in Placebo Patients Risk Difference: Additional Drug Patients with Events per 1,000 Patients Epilepsy Psychiatric Other Total 1 5.7 1 2.4 3.4 8.5 1.8 4.3 3.5 1.5 1.9 1.8 2.4 2.9 0.9 1.9

Adverse reactions cross-check#

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adverse reactions

6 ADVERSE REACTIONS The following serious and otherwise important adverse reactions are described elsewhere in labeling: Permanent Vision Loss [see BOXED WARNING and Warnings and Precautions (5.1) ] Magnetic Resonance Imaging (MRI) Abnormalities in Infants [see Warnings and Precautions (5.3) ] Neurotoxicity [see Warnings and Precautions (5.4) ] Suicidal Behavior and Ideation [see Warnings and Precautions (5.5) ] Withdrawal of Antiepileptic Drugs (AEDs) [see Warnings and Precautions (5.6) ] Anemia [see Warnings and Precautions (5.7) ] Somnolence and Fatigue [see Warnings and Precautions (5.8) ] Peripheral Neuropathy [see Warnings and Precautions (5.9) ] Weight Gain [see Warnings and Precautions (5.10) ] Edema [see Warnings and Precautions (5.11) ] Refractory Complex Partial Seizures Most common adverse reactions in controlled studies include (incidence ≥5% over placebo): Adults: blurred vision, somnolence, dizziness, abnormal coordination, tremor, and fatigue (6.1) Pediatric patients (3 to 16 years of age): weight gain (6.1) Infantile Spasms (incidence >5% and greater than on placebo ) Somnolence, bronchitis, ear infection, and acute otitis media (6.1) To report SUSPECTED ADVERSE REACTIONS, contact Novadoz Pharmaceuticals LLC at 1-855-668-2369 or FDA at 1-800-FDA-1088 or www.fda.gov/medwatch. 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 rates in the clinical trials of another drug and may not reflect the rates observed in practice. In U.S. and primary non-U.S. clinical studies of 4,079 vigabatrin treated patients, the most common (≥5%) adverse reactions associated with the use of vigabatrin in combination with other AEDs were headache, somnolence, fatigue, dizziness, convulsion, nasopharyngitis, weight gain, upper respiratory tract infection, visual field defect, depression, tremor, nystagmus, nausea, diarrhea, memory impairment, insomnia, irritability, abnormal coordination, blurred vision, diplopia, vomiting, influenza, pyrexia, and rash. The adverse reactions most commonly associated with vigabatrin treatment discontinuation in ≥1% of patients were convulsion and depression. In patients with infantile spasms, the adverse reactions most commonly associated with vigabatrin treatment discontinuation in ≥1% ...

adverse reactions table

Vigabatrin dosage (mg/day) Body System Adverse Reaction 3,000 [N=134] % 6,000 [N=43] % Placeb [N=135] % Ear Disorders Tinnitus 2 0 1 Vertigo 2 5 1 Eye Disorders Blurred vision 13 16 5 Diplopia 7 16 3 Asthenopia 2 2 0 Eye pain 0 5 0 Gastrointestinal Disorders Diarrhea 10 16 7 Nausea 10 2 8 Vomiting 7 9 6 Constipation 8 5 3 Upper abdominal pain 5 5 1 Dyspepsia 4 5 3 Stomach discomfort 4 2 1 Abdominal pain 3 2 1 Toothache 2 5 2 Abdominal distension 2 0 1 General Disorders Fatigue 23 40 16 Gait disturbance 6 12 7 Asthenia 5 7 1 Edema peripheral 5 7 1 Fever 4 7 3 Chest pain 1 5 1 Thirst 2 0 0 Malaise 0 5 0 Infections Nasopharyngitis 14 9 10 Upper respiratory tract infection 7 9 6 Influenza 5 7 4 Urinary tract infection 4 5 0 Bronchitis 0 5 1 Injury Contusion 3 5 2 Joint sprain 1 2 1 Muscle strain 1 2 1 Wound secretion 0 2 0 Metabolism and Nutrition Disorders Increased appetite 1 5 1 Weight gain 6 14 3 Musculoskeletal Disorders Arthralgia 10

NDC Listings For This Application#

NDC, Name, Nonproprietary name table
NDCNameNonproprietary nameLabelerMarketing categoryStatus
70377-089VIGABATRINVIGABATRINBiocon Pharma Inc.ANDACurrent
70377-089VIGABATRINVIGABATRINBiocon Pharma Inc.ANDACurrent
72158-101VIGABATRINVIGABATRINNavisci Pte. Ltd.ANDACurrent