FDA NDC Directory · JSON-LD · Markdown

Hydroxyzine Hydrochloride

NDC 70954-912 · HUMAN PRESCRIPTION DRUG · SOLUTION

Labeler / ManufacturerANI Pharmaceuticals, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA219648
Dosage form / routeSOLUTION · ORAL
Active ingredientsHYDROXYZINE DIHYDROCHLORIDE (10 mg/5mL)
Marketing started20260115
Package count1

External sources

Source: openFDA. Public-domain (CC0).