FDA NDC Directory · JSON-LD · Markdown

Fexofenadine hydrochloride

NDC 68001-440 · HUMAN OTC DRUG · TABLET

Labeler / ManufacturerBluePoint Laboratories
Marketing categoryAbbreviated NDA (generic) · App ANDA076502
Dosage form / routeTABLET · ORAL
Active ingredientsFEXOFENADINE HYDROCHLORIDE (180 mg/1)
Marketing started20200619
Package count2

External sources

Source: openFDA. Public-domain (CC0).