FDA NDC Directory · JSON-LD · Markdown

Allergy Relief

NDC 21130-784 · HUMAN OTC DRUG · TABLET

Generic nameFexofenadine hydrochloride
Labeler / ManufacturerSafeway Inc
Marketing categoryAbbreviated NDA (generic) · App ANDA076502
Dosage form / routeTABLET · ORAL
Active ingredientsFEXOFENADINE HYDROCHLORIDE (180 mg/1)
Marketing started20130422
Package count2

External sources

Source: openFDA. Public-domain (CC0).