FDA NDC Directory · JSON-LD · Markdown

Allergy Relief

NDC 30142-856 · HUMAN OTC DRUG · TABLET, COATED

Generic namefexofenadine hydrochloride
Labeler / ManufacturerKroger Company
Marketing categoryAbbreviated NDA (generic) · App ANDA212971
Dosage form / routeTABLET, COATED · ORAL
Active ingredientsFEXOFENADINE HYDROCHLORIDE (180 mg/1)
Marketing started20260625
Package count1

External sources

Source: openFDA. Public-domain (CC0).