FDA NDC Directory · JSON-LD · Markdown

Cetirizine Hydrochloride

NDC 51672-2106 · HUMAN OTC DRUG · SOLUTION

Labeler / ManufacturerTaro Pharmaceuticals U.S.A., Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA201546
Dosage form / routeSOLUTION · ORAL
Active ingredientsCETIRIZINE HYDROCHLORIDE (1 mg/mL)
Marketing started20110520
Package count3

External sources

Source: openFDA. Public-domain (CC0).