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Allergy Relief

NDC 46122-462 · HUMAN OTC DRUG · TABLET

Generic nameFexofenadine hydrochloride
Labeler / ManufacturerAMERISOURCEBERGEN DRUG CORPORATION
Marketing categoryAbbreviated NDA (generic) · App ANDA076502
Dosage form / routeTABLET · ORAL
Active ingredientsFEXOFENADINE HYDROCHLORIDE (180 mg/1)
Marketing started20180220
Marketing ended20260731
Package count2

External sources

Source: openFDA. Public-domain (CC0).