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Fexofenadine hydrochloride

NDC 10202-229 · HUMAN OTC DRUG · TABLET, FILM COATED

Labeler / Manufacturer7-eleven
Marketing categoryAbbreviated NDA (generic) · App ANDA202039
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsFEXOFENADINE HYDROCHLORIDE (180 mg/1)
Marketing started20150115
Package count1

External sources

Source: openFDA. Public-domain (CC0).