FDA NDC Directory · JSON-LD · Markdown

Primidone

NDC 0591-5321 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerActavis Pharma, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA083551
Dosage form / routeTABLET · ORAL
Active ingredientsPRIMIDONE (250 mg/1)
Marketing started20100619
Package count1

External sources

Source: openFDA. Public-domain (CC0).