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Topiramate

NDC 68462-110 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerGlenmark Pharmaceuticals Inc., USA
Marketing categoryAbbreviated NDA (generic) · App ANDA077627
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsTOPIRAMATE (200 mg/1)
Marketing started20090327
Package count3

External sources

Source: openFDA. Public-domain (CC0).