FDA NDC Directory · JSON-LD · Markdown

Primidone

NDC 52817-117 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerTruPharma LLC.
Marketing categoryAbbreviated NDA (generic) · App ANDA214896
Dosage form / routeTABLET · ORAL
Active ingredientsPRIMIDONE (125 mg/1)
Marketing started20220628
Package count3

External sources

Source: openFDA. Public-domain (CC0).