FDA NDC Directory · JSON-LD · Markdown

Fexofenadine

NDC 73581-012 · HUMAN OTC DRUG · TABLET

Labeler / ManufacturerYYBA Corp
Marketing categoryAbbreviated NDA (generic) · App ANDA219032
Dosage form / routeTABLET · ORAL
Active ingredientsFEXOFENADINE HYDROCHLORIDE (60 mg/1)
Marketing started20260727
Package count3

External sources

Source: openFDA. Public-domain (CC0).