FDA NDC Directory · JSON-LD · Markdown

Cetirizine Hydrochloride

NDC 85293-001 · HUMAN OTC DRUG · TABLET

Labeler / ManufacturerUmasuto, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA077829
Dosage form / routeTABLET · ORAL
Active ingredientsCETIRIZINE HYDROCHLORIDE (10 mg/1)
Marketing started20250304
Package count1

External sources

Source: openFDA. Public-domain (CC0).