"71335-0999-1" National Drug Code (NDC)

Olmesartan Medoxomil 30 TABLET, FILM COATED in 1 BOTTLE (71335-0999-1)
(Bryant Ranch Prepack)

NDC Code71335-0999-1
Package Description30 TABLET, FILM COATED in 1 BOTTLE (71335-0999-1)
Product NDC71335-0999
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameOlmesartan Medoxomil
Non-Proprietary NameOlmesartan Medoxomil
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20180823
Marketing Category NameANDA
Application NumberANDA203281
ManufacturerBryant Ranch Prepack
Substance NameOLMESARTAN MEDOXOMIL
Strength40
Strength Unitmg/1
Pharmacy ClassesAngiotensin 2 Receptor Antagonists [MoA], Angiotensin 2 Receptor Blocker [EPC]

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