FDA NDC Directory · JSON-LD · Markdown

FEXOFENADINE HYDROCHLORIDE

NDC 72090-010 · HUMAN OTC DRUG · TABLET

Labeler / ManufacturerPioneer Life Sciences, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA210137
Dosage form / routeTABLET · ORAL
Active ingredientsFEXOFENADINE HYDROCHLORIDE (180 mg/1)
Marketing started20231207
Package count1

External sources

Source: openFDA. Public-domain (CC0).