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Haloperidol

NDC 27241-269 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerAjanta Pharma USA Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA218210
Dosage form / routeTABLET · ORAL
Active ingredientsHALOPERIDOL (20 mg/1)
Marketing started20260914
Package count1

External sources

Source: openFDA. Public-domain (CC0).