FDA NDC Directory · JSON-LD · Markdown

VIGABATRIN

NDC 67877-674 · HUMAN PRESCRIPTION DRUG · POWDER, FOR SOLUTION

Labeler / ManufacturerAscend Laboratories, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA213375
Dosage form / routePOWDER, FOR SOLUTION · ORAL
Active ingredientsVIGABATRIN (50 mg/mL)
Marketing started20201203
Package count1

External sources

Source: openFDA. Public-domain (CC0).