FDA NDC Directory · JSON-LD · Markdown

Fexofenadine Hydrochloride

NDC 84324-045 · HUMAN OTC DRUG · TABLET

Labeler / ManufacturerNUVICARE LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA204507
Dosage form / routeTABLET · ORAL
Active ingredientsFEXOFENADINE HYDROCHLORIDE (60 mg/1)
Marketing started20260730
Package count1

External sources

Source: openFDA. Public-domain (CC0).