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Fexofenadine Hydrochloride

NDC 45802-847 · HUMAN OTC DRUG · TABLET, FILM COATED

Generic namefexofenadine hydrochloride
Labeler / ManufacturerPadagis Israel Pharmaceuticals Ltd
Marketing categoryAbbreviated NDA (generic) · App ANDA212971
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsFEXOFENADINE HYDROCHLORIDE (180 mg/1)
Marketing started20220107
Package count1

External sources

Source: openFDA. Public-domain (CC0).