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Haloperidol

NDC 0904-7504 · HUMAN PRESCRIPTION DRUG · TABLET

Generic namehaloperidol
Labeler / ManufacturerMajor Pharmaceuticals
Marketing categoryAbbreviated NDA (generic) · App ANDA216918
Dosage form / routeTABLET · ORAL
Active ingredientsHALOPERIDOL (2 mg/1)
Marketing started20250128
Package count1

External sources

Source: openFDA. Public-domain (CC0).