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HYDROXYZINE HYDROCHLORIDE

NDC 10135-810 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Generic namehydroxyzine hydrochloride
Labeler / ManufacturerMarlex Pharmaceuticals, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA207121
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsHYDROXYZINE DIHYDROCHLORIDE (10 mg/1)
Marketing started20250301
Package count2

External sources

Source: openFDA. Public-domain (CC0).