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Hydroxyzine Hydrochloride

NDC 50090-4117 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerA-S Medication Solutions
Marketing categoryAbbreviated NDA (generic) · App ANDA088617
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsHYDROXYZINE DIHYDROCHLORIDE (10 mg/1)
Marketing started20130219
Package count2

External sources

Source: openFDA. Public-domain (CC0).