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Primidone

NDC 55111-477 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerDr. Reddy's Laboratories Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA040862
Dosage form / routeTABLET · ORAL
Active ingredientsPRIMIDONE (50 mg/1)
Marketing started20081003
Package count5

External sources

Source: openFDA. Public-domain (CC0).