# Vigabatrin

NDC: 42799-950
Generic name: Vigabatrin
Labeler / Manufacturer: Edenbridge Pharmaceuticals LLC.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20220629

FDA application: ANDA215109

## 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:"42799-950"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=42799-950
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=93ba3894-fd97-4432-9f2d-e7050371e91f