FDA NDC Directory · JSON-LD · Markdown

Cetirizine Hydrochloride

NDC 68016-939 · HUMAN OTC DRUG · TABLET

Labeler / ManufacturerChain Drug Consortium, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA077498
Dosage form / routeTABLET · ORAL
Active ingredientsCETIRIZINE HYDROCHLORIDE (10 mg/1)
Marketing started20071227
Package count4

External sources

Source: openFDA. Public-domain (CC0).