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Primidone

NDC 65162-545 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerAmneal Pharmaceuticals LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA040866
Dosage form / routeTABLET · ORAL
Active ingredientsPRIMIDONE (250 mg/1)
Marketing started20091224
Package count3

External sources

Source: openFDA. Public-domain (CC0).