FDA NDC Directory · JSON-LD · Markdown

Sumatriptan

NDC 68788-6769 · HUMAN PRESCRIPTION DRUG · TABLET

Generic nameSumatriptan Succinate
Labeler / ManufacturerPreferred Pharmaceuticals Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA078327
Dosage form / routeTABLET · ORAL
Active ingredientsSUMATRIPTAN SUCCINATE (25 mg/1)
Marketing started20161024
Package count1

External sources

Source: openFDA. Public-domain (CC0).