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fexofenadine hcl

NDC 0904-7192 · HUMAN OTC DRUG · TABLET, FILM COATED

Labeler / ManufacturerMajor Pharmaceuticals
Marketing categoryAbbreviated NDA (generic) · App ANDA204507
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsFEXOFENADINE HYDROCHLORIDE (60 mg/1)
Marketing started20210826
Package count3

External sources

Source: openFDA. Public-domain (CC0).