"70771-1059-7" National Drug Code (NDC)

Olmesartan Medoxomil 10 BLISTER PACK in 1 CARTON (70771-1059-7) > 10 TABLET, FILM COATED in 1 BLISTER PACK (70771-1059-2)
(Zydus Lifesciences Limited)

NDC Code70771-1059-7
Package Description10 BLISTER PACK in 1 CARTON (70771-1059-7) > 10 TABLET, FILM COATED in 1 BLISTER PACK (70771-1059-2)
Product NDC70771-1059
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameOlmesartan Medoxomil
Non-Proprietary NameOlmesartan Medoxomil
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20170424
Marketing Category NameANDA
Application NumberANDA205192
ManufacturerZydus Lifesciences Limited
Substance NameOLMESARTAN MEDOXOMIL
Strength5
Strength Unitmg/1
Pharmacy ClassesAngiotensin 2 Receptor Antagonists [MoA], Angiotensin 2 Receptor Blocker [EPC]

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