FDA NDC Directory · JSON-LD · Markdown

Fexofenadine Hydrochloride

NDC 63868-025 · HUMAN OTC DRUG · TABLET

Generic nameFexofenadine hydrochloride
Labeler / ManufacturerChain Drug Marketing Associate
Marketing categoryAbbreviated NDA (generic) · App ANDA076502
Dosage form / routeTABLET · ORAL
Active ingredientsFEXOFENADINE HYDROCHLORIDE (180 mg/1)
Marketing started20140401
Package count1

External sources

Source: openFDA. Public-domain (CC0).