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Sumatriptan

NDC 80425-0224 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerAdvanced Rx of Tennessee, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA078327
Dosage form / routeTABLET · ORAL
Active ingredientsSUMATRIPTAN SUCCINATE (100 mg/1)
Marketing started20230112
Package count1

External sources

Source: openFDA. Public-domain (CC0).