FDA NDC Directory · JSON-LD · Markdown

Hydroxyzine hydrochloride

NDC 70518-2807 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerREMEDYREPACK INC.
Marketing categoryAbbreviated NDA (generic) · App ANDA204279
Dosage form / routeTABLET · ORAL
Active ingredientsHYDROXYZINE DIHYDROCHLORIDE (10 mg/1)
Marketing started20200708
Package count1

External sources

Source: openFDA. Public-domain (CC0).