FDA NDC Directory · JSON-LD · Markdown

Fexofenadine Hydrochloride

NDC 58602-426 · HUMAN OTC DRUG · SUSPENSION

Generic nameFexofenadine Hydrochloride Oral
Labeler / ManufacturerAurohealth LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA213466
Dosage form / routeSUSPENSION · ORAL
Active ingredientsFEXOFENADINE HYDROCHLORIDE (30 mg/5mL)
Marketing started20230523
Package count2

External sources

Source: openFDA. Public-domain (CC0).