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Primidone

NDC 72888-045 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerAdvagen Pharma Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA214896
Dosage form / routeTABLET · ORAL
Active ingredientsPRIMIDONE (50 mg/1)
Marketing started20220628
Package count2

External sources

Source: openFDA. Public-domain (CC0).