"65862-671-05" National Drug Code (NDC)

Repaglinide 500 TABLET in 1 BOTTLE (65862-671-05)
(Aurobindo Pharma Limited)

NDC Code65862-671-05
Package Description500 TABLET in 1 BOTTLE (65862-671-05)
Product NDC65862-671
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameRepaglinide
Non-Proprietary NameRepaglinide
Dosage FormTABLET
UsageORAL
Start Marketing Date20140122
Marketing Category NameANDA
Application NumberANDA203820
ManufacturerAurobindo Pharma Limited
Substance NameREPAGLINIDE
Strength1
Strength Unitmg/1
Pharmacy ClassesGlinide [EPC], Potassium Channel Antagonists [MoA]

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