FDA NDC Directory · JSON-LD · Markdown

FEXOFENADINE HYDROCHLORIDE

NDC 51660-998 · HUMAN OTC DRUG · TABLET, FILM COATED

Labeler / ManufacturerOHM LABORATORIES INC.
Marketing categoryAbbreviated NDA (generic) · App ANDA091567
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsFEXOFENADINE HYDROCHLORIDE (180 mg/1)
Marketing started20220429
Package count2

External sources

Source: openFDA. Public-domain (CC0).