FDA NDC Directory · JSON-LD · Markdown

Topiramate

NDC 51655-608 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerNorthwind Health Company, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA077627
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsTOPIRAMATE (100 mg/1)
Marketing started20150202
Package count2

External sources

Source: openFDA. Public-domain (CC0).