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HALOPERIDOL

NDC 72205-067 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerNovadoz Pharmaceuticals LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA216004
Dosage form / routeTABLET · ORAL
Active ingredientsHALOPERIDOL (5 mg/1)
Marketing started20221118
Package count2

External sources

Source: openFDA. Public-domain (CC0).