FDA NDC Directory · JSON-LD · Markdown

Fexofenadine Hydrochloride

NDC 62207-891 · HUMAN OTC DRUG · TABLET, FILM COATED

Labeler / ManufacturerGranules India Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA211075
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsFEXOFENADINE HYDROCHLORIDE (180 mg/1)
Marketing started20231107
Package count3

External sources

Source: openFDA. Public-domain (CC0).