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Fexofenadine hydrochloride

NDC 55111-783 · HUMAN OTC DRUG · TABLET

Labeler / ManufacturerDr. Reddy's Laboratories Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA076502
Dosage form / routeTABLET · ORAL
Active ingredientsFEXOFENADINE HYDROCHLORIDE (60 mg/1)
Marketing started20110103
Package count6

External sources

Source: openFDA. Public-domain (CC0).