FDA NDC Directory · JSON-LD · Markdown

Allergy Relief

NDC 68016-294 · HUMAN OTC DRUG · TABLET, COATED

Generic nameCetirizine hydrochloride
Labeler / ManufacturerCHAIN DRUG CONSORTIUM
Marketing categoryAbbreviated NDA (generic) · App ANDA209274
Dosage form / routeTABLET, COATED · ORAL
Active ingredientsCETIRIZINE HYDROCHLORIDE (10 mg/1)
Marketing started20191101
Marketing ended20260731
Package count3

External sources

Source: openFDA. Public-domain (CC0).