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"57664-747-18" National Drug Code (NDC)

Repaglinide 1000 TABLET in 1 BOTTLE (57664-747-18)
(Sun Pharmaceutical Industries, Inc.)

NDC Code57664-747-18
Package Description1000 TABLET in 1 BOTTLE (57664-747-18)
Product NDC57664-747
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameRepaglinide
Non-Proprietary NameRepaglinide
Dosage FormTABLET
UsageORAL
Start Marketing Date20130711
Marketing Category NameANDA
Application NumberANDA077571
ManufacturerSun Pharmaceutical Industries, Inc.
Substance NameREPAGLINIDE
Strength2
Strength Unitmg/1
Pharmacy ClassesGlinide [EPC], Potassium Channel Antagonists [MoA]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/57664-747-18





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