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Childrens Fexofenadine Hydrochloride Allergy

NDC 51672-2141 · HUMAN OTC DRUG · SUSPENSION

Generic nameFEXOFENADINE HYDROCHLORIDE
Labeler / ManufacturerSun Pharmaceutical Industries, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA208123
Dosage form / routeSUSPENSION · ORAL
Active ingredientsFEXOFENADINE HYDROCHLORIDE (30 mg/5mL)
Marketing started20240124
Package count2

External sources

Source: openFDA. Public-domain (CC0).