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FEXOFENADINE HCl

NDC 70677-1239 · HUMAN OTC DRUG · TABLET, FILM COATED

Labeler / ManufacturerStrategic Sourcing Services, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA210137
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsFEXOFENADINE HYDROCHLORIDE (180 mg/1)
Marketing started20240222
Package count1

External sources

Source: openFDA. Public-domain (CC0).