FDA NDC Directory · JSON-LD · Markdown

allergy relief

NDC 37808-583 · HUMAN OTC DRUG · TABLET, FILM COATED

Generic nameCetirizine Hydrochloride
Labeler / ManufacturerH E B
Marketing categoryAbbreviated NDA (generic) · App ANDA078336
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsCETIRIZINE HYDROCHLORIDE (10 mg/1)
Marketing started20180126
Package count4

External sources

Source: openFDA. Public-domain (CC0).