FDA NDC Directory · JSON-LD · Markdown

Hydroxyzine Hydrochloride

NDC 71656-090 · HUMAN PRESCRIPTION DRUG · SOLUTION

Labeler / ManufacturerSaptalis Pharmaceuticals, LLC.
Marketing categoryAbbreviated NDA (generic) · App ANDA220271
Dosage form / routeSOLUTION · ORAL
Active ingredientsHYDROXYZINE HYDROCHLORIDE (10 mg/5mL)
Marketing started20260617
Package count1

External sources

Source: openFDA. Public-domain (CC0).