FDA NDC Directory · JSON-LD · Markdown

fexofenadine hcl

NDC 71335-2165 · HUMAN OTC DRUG · TABLET, FILM COATED

Labeler / ManufacturerBryant Ranch Prepack
Marketing categoryAbbreviated NDA (generic) · App ANDA204507
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsFEXOFENADINE HYDROCHLORIDE (60 mg/1)
Marketing started20210826
Package count7

External sources

Source: openFDA. Public-domain (CC0).