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Hydroxyzine Hydrochloride

NDC 60687-875 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerAmerican Health Packaging
Marketing categoryAbbreviated NDA (generic) · App ANDA087871
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsHYDROXYZINE DIHYDROCHLORIDE (50 mg/1)
Marketing started20250911
Package count1

External sources

Source: openFDA. Public-domain (CC0).