FDA NDC Directory · JSON-LD · Markdown

Sumatriptan

NDC 69452-345 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerBionpharma Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA078284
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsSUMATRIPTAN SUCCINATE (50 mg/1)
Marketing started20220218
Package count1

External sources

Source: openFDA. Public-domain (CC0).