FDA NDC Directory · JSON-LD · Markdown

Allergy Relief

NDC 59726-701 · HUMAN OTC DRUG · TABLET, COATED

Generic nameFexofenadine HCl
Labeler / ManufacturerP & L Development, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA204507
Dosage form / routeTABLET, COATED · ORAL
Active ingredientsFEXOFENADINE HYDROCHLORIDE (180 mg/1)
Marketing started20210820
Package count1

External sources

Source: openFDA. Public-domain (CC0).