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Hydroxyzine Hydrochloride

NDC 10702-012 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerKVK-Tech, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA040786
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsHYDROXYZINE DIHYDROCHLORIDE (50 mg/1)
Marketing started20120724
Package count3

External sources

Source: openFDA. Public-domain (CC0).