FDA NDC Directory · JSON-LD · Markdown

allergy relief

NDC 41163-292 · HUMAN OTC DRUG · TABLET

Generic nameFexofenadine Hydrochloride
Labeler / ManufacturerUnited Natural Foods, Inc. dba UNFI
Marketing categoryAbbreviated NDA (generic) · App ANDA211075
Dosage form / routeTABLET · ORAL
Active ingredientsFEXOFENADINE HYDROCHLORIDE (180 mg/1)
Marketing started20211029
Package count3

External sources

Source: openFDA. Public-domain (CC0).