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Fexofenadine hydrochloride

NDC 0904-6711 · HUMAN OTC DRUG · TABLET

Labeler / ManufacturerMAJOR PHARMACEUTICALS
Marketing categoryAbbreviated NDA (generic) · App ANDA076502
Dosage form / routeTABLET · ORAL
Active ingredientsFEXOFENADINE HYDROCHLORIDE (180 mg/1)
Marketing started20180427
Marketing ended20260831
Package count1

External sources

Source: openFDA. Public-domain (CC0).