FDA NDC Directory · JSON-LD · Markdown

topiramate

NDC 68788-8835 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerPreferred Pharmaceuticals Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA090162
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsTOPIRAMATE (100 mg/1)
Marketing started20250221
Package count4

External sources

Source: openFDA. Public-domain (CC0).