# VIGABATRIN

NDC: 67877-674
Generic name: VIGABATRIN
Labeler / Manufacturer: Ascend Laboratories, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: POWDER, FOR SOLUTION
Routes: ORAL
Marketing started: 20201203

FDA application: ANDA213375

## 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:"67877-674"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=67877-674
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=ee835fb6-2b2b-40c4-b6d7-0ad0e790cda8