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"65862-672-99" National Drug Code (NDC)

Repaglinide 1000 TABLET in 1 BOTTLE (65862-672-99)
(Aurobindo Pharma Limited)

NDC Code65862-672-99
Package Description1000 TABLET in 1 BOTTLE (65862-672-99)
Product NDC65862-672
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
Strength2
Strength Unitmg/1
Pharmacy ClassesGlinide [EPC], Potassium Channel Antagonists [MoA]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/65862-672-99





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