FDA NDC Directory · JSON-LD · Markdown

Fexofenadine hydrochloride

NDC 55111-784 · HUMAN OTC DRUG · TABLET

Labeler / ManufacturerDr. Reddy's Laboratories Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA076502
Dosage form / routeTABLET · ORAL
Active ingredientsFEXOFENADINE HYDROCHLORIDE (180 mg/1)
Marketing started20110103
Package count17

External sources

Source: openFDA. Public-domain (CC0).