FDA NDC Directory · JSON-LD · Markdown

Non-Drowsy Allergy Relief

NDC 11673-621 · HUMAN OTC DRUG · TABLET

Generic nameFexofenadine hydrochloride
Labeler / ManufacturerTARGET CORPORATION
Marketing categoryAbbreviated NDA (generic) · App ANDA076502
Dosage form / routeTABLET · ORAL
Active ingredientsFEXOFENADINE HYDROCHLORIDE (180 mg/1)
Marketing started20250801
Package count5

External sources

Source: openFDA. Public-domain (CC0).