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Crcle Fexofenadine Hydrochloride

NDC 57483-240 · HUMAN OTC DRUG · TABLET

Generic nameFexofenadine Hydrochloride
Labeler / ManufacturerInnovus Pharmaceuticals, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA211075
Dosage form / routeTABLET · ORAL
Active ingredientsFEXOFENADINE HYDROCHLORIDE (180 mg/1)
Marketing started20201218
Package count1

External sources

Source: openFDA. Public-domain (CC0).