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Haloperidol

NDC 68382-409 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerZydus Pharmaceuticals USA Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA077580
Dosage form / routeTABLET · ORAL
Active ingredientsHALOPERIDOL (2 mg/1)
Marketing started20230201
Package count3

External sources

Source: openFDA. Public-domain (CC0).