FDA NDC Directory · JSON-LD · Markdown

Primidone

NDC 69584-685 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerOxford Pharmaceuticals, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA040586
Dosage form / routeTABLET · ORAL
Active ingredientsPRIMIDONE (250 mg/1)
Marketing started20210222
Package count2

External sources

Source: openFDA. Public-domain (CC0).