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Hydroxyzine Hydrochloride

NDC 55154-7994 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerCardinal Health 107, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA040604
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsHYDROXYZINE DIHYDROCHLORIDE (25 mg/1)
Marketing started20150331
Marketing ended20260831
Package count1

External sources

Source: openFDA. Public-domain (CC0).