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Haloperidol

NDC 72789-558 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerPD-Rx Pharmaceuticals, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA071130
Dosage form / routeTABLET · ORAL
Active ingredientsHALOPERIDOL (5 mg/1)
Marketing started20260408
Package count1

External sources

Source: openFDA. Public-domain (CC0).