FDA NDC Directory · JSON-LD · Markdown

FEXOFENADINE HYDROCHLORIDE

NDC 51316-800 · HUMAN OTC DRUG · TABLET

Labeler / ManufacturerCVS PHARMACY, INC
Marketing categoryAbbreviated NDA (generic) · App ANDA091567
Dosage form / routeTABLET · ORAL
Active ingredientsFEXOFENADINE HYDROCHLORIDE (180 mg/1)
Marketing started20220920
Package count6

External sources

Source: openFDA. Public-domain (CC0).