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Topiramate

NDC 68084-345 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerAmerican Health Packaging
Marketing categoryAbbreviated NDA (generic) · App ANDA078235
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsTOPIRAMATE (200 mg/1)
Marketing started20090413
Package count1

External sources

Source: openFDA. Public-domain (CC0).