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telmisartan

NDC 68382-473 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerZydus Pharmaceuticals USA Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA203325
Dosage form / routeTABLET · ORAL
Active ingredientsTELMISARTAN (80 mg/1)
Marketing started20140827
Package count6

External sources

Source: openFDA. Public-domain (CC0).