FDA NDC Directory · JSON-LD · Markdown

topiramate

NDC 68788-7351 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerPreferred Pharmaceuticals Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA078235
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsTOPIRAMATE (50 mg/1)
Marketing started20190227
Package count5

External sources

Source: openFDA. Public-domain (CC0).