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Primidone

NDC 82804-952 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerProficient Rx LP
Marketing categoryAbbreviated NDA (generic) · App ANDA040586
Dosage form / routeTABLET · ORAL
Active ingredientsPRIMIDONE (50 mg/1)
Marketing started20210222
Package count7

External sources

Source: openFDA. Public-domain (CC0).