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Fexofenadine Hydrochloride

NDC 51655-231 · HUMAN OTC DRUG · TABLET

Generic nameFexofenadine HCl
Labeler / ManufacturerNorthwind Health Company, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA204507
Dosage form / routeTABLET · ORAL
Active ingredientsFEXOFENADINE HYDROCHLORIDE (180 mg/1)
Marketing started20221116
Marketing ended20261028
Package count2

External sources

Source: openFDA. Public-domain (CC0).