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Telmisartan

NDC 53746-293 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerAmneal Pharmaceuticals of New York LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA204415
Dosage form / routeTABLET · ORAL
Active ingredientsTELMISARTAN (80 mg/1)
Marketing started20160925
Package count1

External sources

Source: openFDA. Public-domain (CC0).