FDA NDC Directory · JSON-LD · Markdown

Allergy Relief

NDC 68210-4159 · HUMAN OTC DRUG · TABLET, FILM COATED

Generic nameCetirizine Hydrochloride
Labeler / ManufacturerProdose, Inc
Marketing categoryAbbreviated NDA (generic) · App ANDA077829
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsCETIRIZINE HYDROCHLORIDE (10 mg/1)
Marketing started20210428
Package count1

External sources

Source: openFDA. Public-domain (CC0).