FDA NDC Directory · JSON-LD · Markdown

Sumatriptan

NDC 63304-099 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerSUN PHARMACEUTICAL INDUSTRIES, INC.
Marketing categoryAbbreviated NDA (generic) · App ANDA076572
Dosage form / routeTABLET · ORAL
Active ingredientsSUMATRIPTAN SUCCINATE (100 mg/1)
Marketing started20090210
Package count3

External sources

Source: openFDA. Public-domain (CC0).