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HALOPERIDOL

NDC 82619-110 · HUMAN PRESCRIPTION DRUG · TABLET

Generic namehaloperidol
Labeler / ManufacturerCreekwood Pharmaceuticals LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA218162
Dosage form / routeTABLET · ORAL
Active ingredientsHALOPERIDOL (20 mg/1)
Marketing started20260105
Package count2

External sources

Source: openFDA. Public-domain (CC0).