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Hydroxyzine Hydrochloride

NDC 43063-960 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Generic namehydroxyzine hydrochloride
Labeler / ManufacturerPD-Rx Pharmaceuticals, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA040786
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsHYDROXYZINE DIHYDROCHLORIDE (10 mg/1)
Marketing started20120724
Package count2

External sources

Source: openFDA. Public-domain (CC0).