FDA NDC Directory · JSON-LD · Markdown

Fexofenadine HCL

NDC 79481-6230 · HUMAN OTC DRUG · TABLET

Labeler / ManufacturerMeijer, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA211075
Dosage form / routeTABLET · ORAL
Active ingredientsFEXOFENADINE HYDROCHLORIDE (180 mg/1)
Marketing started20240701
Package count2

External sources

Source: openFDA. Public-domain (CC0).