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Hydroxyzine Hydrochloride

NDC 24658-783 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerPURACAP LABORATORIES LLC DBA BLU PHARMACEUTICALS
Marketing categoryAbbreviated NDA (generic) · App ANDA040604
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsHYDROXYZINE DIHYDROCHLORIDE (50 mg/1)
Marketing started20210721
Package count1

External sources

Source: openFDA. Public-domain (CC0).