FDA NDC Directory · JSON-LD · Markdown

PRIMIDONE

NDC 72189-216 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerDIRECT RX
Marketing categoryAbbreviated NDA (generic) · App ANDA040586
Dosage form / routeTABLET · ORAL
Active ingredientsPRIMIDONE (50 mg/1)
Marketing started20210511
Package count1

External sources

Source: openFDA. Public-domain (CC0).