FDA NDC Directory · JSON-LD · Markdown

Allergy Relief non drowsy

NDC 41250-506 · HUMAN OTC DRUG · TABLET, COATED

Generic nameFexofenadine HCl
Labeler / ManufacturerMEIJER, INC.
Marketing categoryAbbreviated NDA (generic) · App ANDA204507
Dosage form / routeTABLET, COATED · ORAL
Active ingredientsFEXOFENADINE HYDROCHLORIDE (180 mg/1)
Marketing started20180331
Marketing ended20261231
Package count4

External sources

Source: openFDA. Public-domain (CC0).