FDA NDC Directory · JSON-LD · Markdown

Cetirizine Hydrochloride

NDC 51672-4070 · HUMAN PRESCRIPTION DRUG · SOLUTION

Labeler / ManufacturerSun Pharmaceutical Industries, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA076601
Dosage form / routeSOLUTION · ORAL
Active ingredientsCETIRIZINE HYDROCHLORIDE (1 mg/mL)
Marketing started20140501
Package count1

External sources

Source: openFDA. Public-domain (CC0).