FDA NDC Directory · JSON-LD · Markdown

vigabatrin

NDC 70771-1742 · HUMAN PRESCRIPTION DRUG · POWDER, FOR SOLUTION

Labeler / ManufacturerZydus Lifesciences Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA214671
Dosage form / routePOWDER, FOR SOLUTION · ORAL
Active ingredientsVIGABATRIN (500 mg/10mL)
Marketing started20250324
Package count1

External sources

Source: openFDA. Public-domain (CC0).