FDA NDC Directory · JSON-LD · Markdown

allergy relief

NDC 79481-0847 · HUMAN OTC DRUG · TABLET, FILM COATED

Generic namefexofenadine hydrochloride
Labeler / ManufacturerMeijer, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA212971
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsFEXOFENADINE HYDROCHLORIDE (180 mg/1)
Marketing started20211006
Package count5

External sources

Source: openFDA. Public-domain (CC0).