FDA NDC Directory · JSON-LD · Markdown

Fexofenadine HCL

NDC 70677-1256 · HUMAN OTC DRUG · TABLET

Labeler / ManufacturerStrategic Sourcing Services
Marketing categoryAbbreviated NDA (generic) · App ANDA204097
Dosage form / routeTABLET · ORAL
Active ingredientsFEXOFENADINE HYDROCHLORIDE (180 mg/1)
Marketing started20250501
Package count2

External sources

Source: openFDA. Public-domain (CC0).