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Fexofenadine Hydrochloride

NDC 43598-936 · HUMAN OTC DRUG · TABLET

Generic nameFexofenadine hydrochloride
Labeler / ManufacturerDr. Reddy's Laboratories Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA076502
Dosage form / routeTABLET · ORAL
Active ingredientsFEXOFENADINE HYDROCHLORIDE (60 mg/1)
Marketing started20201201
Package count1

External sources

Source: openFDA. Public-domain (CC0).