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HYDROXYZINE HYDROCHLORIDE

NDC 70518-4170 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Generic namehydroxyzine hydrochloride
Labeler / ManufacturerREMEDYREPACK INC.
Marketing categoryAbbreviated NDA (generic) · App ANDA217652
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsHYDROXYZINE DIHYDROCHLORIDE (50 mg/1)
Marketing started20240828
Package count6

External sources

Source: openFDA. Public-domain (CC0).