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Primidone

NDC 0527-1231 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerLannett Company, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA084903
Dosage form / routeTABLET · ORAL
Active ingredientsPRIMIDONE (250 mg/1)
Marketing started19781201
Package count3

External sources

Source: openFDA. Public-domain (CC0).