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Hydroxyzine Hydrochloride

NDC 65162-577 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Generic nameHydroxyzine
Labeler / ManufacturerAmneal Pharmaceuticals LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA040808
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsHYDROXYZINE DIHYDROCHLORIDE (50 mg/1)
Marketing started20080924
Package count3

External sources

Source: openFDA. Public-domain (CC0).