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Haloperidol

NDC 0378-0327 · HUMAN PRESCRIPTION DRUG · TABLET

Generic namehaloperidol
Labeler / ManufacturerMylan Pharmaceuticals Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA070278
Dosage form / routeTABLET · ORAL
Active ingredientsHALOPERIDOL (5 mg/1)
Marketing started19860610
Marketing ended20270331
Package count1

External sources

Source: openFDA. Public-domain (CC0).