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Fexofenadine Hydrochloride

NDC 62207-623 · HUMAN OTC DRUG · TABLET

Labeler / ManufacturerGranules India Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA211075
Dosage form / routeTABLET · ORAL
Active ingredientsFEXOFENADINE HYDROCHLORIDE (180 mg/1)
Marketing started20240102
Package count4

External sources

Source: openFDA. Public-domain (CC0).