FDA NDC Directory · JSON-LD · Markdown

all day allergy

NDC 11822-1002 · HUMAN OTC DRUG · TABLET, FILM COATED

Generic nameCetirizine Hydrochloride
Labeler / ManufacturerRite Aid Corporation
Marketing categoryAbbreviated NDA (generic) · App ANDA078336
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsCETIRIZINE HYDROCHLORIDE (10 mg/1)
Marketing started20210914
Package count6

External sources

Source: openFDA. Public-domain (CC0).