# Vigabatrin

NDC: 59651-366
Generic name: Vigabatrin
Labeler / Manufacturer: Aurobindo Pharma Limited
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: POWDER, FOR SOLUTION
Routes: ORAL
Marketing started: 20210929

FDA application: ANDA213899

## Active ingredients

- VIGABATRIN: 500 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"59651-366"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=59651-366
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=c97ce40c-1c5a-479d-9188-5ce03cf7e065