FDA NDC Directory · JSON-LD · Markdown

Fexofenadine Hydrochloride

NDC 68210-2210 · HUMAN OTC DRUG · TABLET, FILM COATED

Labeler / ManufacturerSPIRIT PHARMACEUTICALS LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA204507
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsFEXOFENADINE HYDROCHLORIDE (180 mg/1)
Marketing started20200317
Package count1

External sources

Source: openFDA. Public-domain (CC0).