"0781-5149-10" National Drug Code (NDC)

Repaglinide 1000 TABLET in 1 BOTTLE (0781-5149-10)
(Sandoz Inc)

NDC Code0781-5149-10
Package Description1000 TABLET in 1 BOTTLE (0781-5149-10)
Product NDC0781-5149
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameRepaglinide
Non-Proprietary NameRepaglinide
Dosage FormTABLET
UsageORAL
Start Marketing Date20140122
Marketing Category NameANDA
Application NumberANDA078555
ManufacturerSandoz Inc
Substance NameREPAGLINIDE
Strength1
Strength Unitmg/1
Pharmacy ClassesGlinide [EPC],Potassium Channel Antagonists [MoA]

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