FDA NDC Directory · JSON-LD · Markdown

Allergy Relief

NDC 37808-392 · HUMAN OTC DRUG · TABLET

Generic nameFexofenadine Hydrochloride
Labeler / ManufacturerHEB
Marketing categoryAbbreviated NDA (generic) · App ANDA211075
Dosage form / routeTABLET · ORAL
Active ingredientsFEXOFENADINE HYDROCHLORIDE (180 mg/1)
Marketing started20220531
Package count5

External sources

Source: openFDA. Public-domain (CC0).