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Haloperidol

NDC 70518-2682 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerREMEDYREPACK INC.
Marketing categoryAbbreviated NDA (generic) · App ANDA071173
Dosage form / routeTABLET · ORAL
Active ingredientsHALOPERIDOL (1 mg/1)
Marketing started20200408
Package count2

External sources

Source: openFDA. Public-domain (CC0).