FDA NDC Directory · JSON-LD · Markdown

FEXOFENADINE HYDROCHLORIDE

NDC 46122-779 · HUMAN OTC DRUG · TABLET, FILM COATED

Labeler / ManufacturerAMERISOURCE BERGEN
Marketing categoryAbbreviated NDA (generic) · App ANDA091567
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsFEXOFENADINE HYDROCHLORIDE (180 mg/1)
Marketing started20240514
Package count3

External sources

Source: openFDA. Public-domain (CC0).