FDA NDC Directory · JSON-LD · Markdown

allergy relief

NDC 0363-4101 · HUMAN OTC DRUG · TABLET, FILM COATED

Generic nameCetirizine Hydrochloride
Labeler / ManufacturerWalgreen Company
Marketing categoryAbbreviated NDA (generic) · App ANDA078336
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsCETIRIZINE HYDROCHLORIDE (10 mg/1)
Marketing started20211021
Package count7

External sources

Source: openFDA. Public-domain (CC0).