"57664-757-99" National Drug Code (NDC)

Olmesartan Medoxomil 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (57664-757-99)
(Sun Pharmaceutical Industries, Inc.)

NDC Code57664-757-99
Package Description90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (57664-757-99)
Product NDC57664-757
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameOlmesartan Medoxomil
Non-Proprietary NameOlmesartan Medoxomil
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20161026
Marketing Category NameNDA AUTHORIZED GENERIC
Application NumberNDA021286
ManufacturerSun Pharmaceutical Industries, Inc.
Substance NameOLMESARTAN MEDOXOMIL
Strength40
Strength Unitmg/1
Pharmacy ClassesAngiotensin 2 Receptor Antagonists [MoA], Angiotensin 2 Receptor Blocker [EPC]

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