FDA NDC Directory · JSON-LD · Markdown

Fexofenadine Hydrochloride

NDC 73629-008 · HUMAN OTC DRUG · TABLET, FILM COATED

Labeler / ManufacturerAMZ789 LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA211075
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsFEXOFENADINE HYDROCHLORIDE (180 mg/1)
Marketing started20240727
Package count1

External sources

Source: openFDA. Public-domain (CC0).