# Vigabatrin

NDC: 43598-697
Generic name: Vigabatrin
Labeler / Manufacturer: Dr. Reddys Laboratories Inc.,
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: POWDER, FOR SOLUTION
Routes: ORAL
Marketing started: 20181121

FDA application: ANDA211481

## Active ingredients

- VIGABATRIN: 50 mg/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"43598-697"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=43598-697
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=f6be436e-46c7-e9ab-0fcf-e8d04dc12b72