FDA NDC Directory · JSON-LD · Markdown

HYDROXYZINE HYDROCHLORIDE

NDC 83745-232 · HUMAN PRESCRIPTION DRUG · SOLUTION

Labeler / ManufacturerAPOZEAL PHARMACEUTICALS INC
Marketing categoryAbbreviated NDA (generic) · App ANDA210634
Dosage form / routeSOLUTION · ORAL
Active ingredientsHYDROXYZINE DIHYDROCHLORIDE (10 mg/5mL)
Marketing started20240716
Package count1

External sources

Source: openFDA. Public-domain (CC0).