FDA NDC Directory · JSON-LD · Markdown

HYDROXYZINE HYDROCHLORIDE

NDC 11534-206 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Generic namehydroxyzine hydrochloride
Labeler / ManufacturerSunrise Pharmaceutical, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA207121
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsHYDROXYZINE DIHYDROCHLORIDE (50 mg/1)
Marketing started20240501
Package count3

External sources

Source: openFDA. Public-domain (CC0).