# vigabatrin for oral solution

NDC: 31722-009
Generic name: vigabatrin
Labeler / Manufacturer: Camber Pharmaceuticals, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: POWDER, FOR SOLUTION
Routes: ORAL
Marketing started: 20210126

FDA application: ANDA213519

## Active ingredients

- VIGABATRIN: 50 mg/mL

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"31722-009"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=31722-009
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=bda491b6-47ba-400b-9816-b6d15c6e2683