FDA NDC Directory · JSON-LD · Markdown

Fexofenadine HCL

NDC 68788-7449 · HUMAN OTC DRUG · TABLET

Labeler / ManufacturerPreferred Pharmaceuticals, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA204097
Dosage form / routeTABLET · ORAL
Active ingredientsFEXOFENADINE HYDROCHLORIDE (180 mg/1)
Marketing started20160819
Package count4

External sources

Source: openFDA. Public-domain (CC0).