"51991-854-01" National Drug Code (NDC)

Repaglinide 100 TABLET in 1 BOTTLE (51991-854-01)
(Breckenridge Pharmaceutical, Inc.)

NDC Code51991-854-01
Package Description100 TABLET in 1 BOTTLE (51991-854-01)
Product NDC51991-854
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameRepaglinide
Non-Proprietary NameRepaglinide
Dosage FormTABLET
UsageORAL
Start Marketing Date20150501
End Marketing Date20220531
Marketing Category NameANDA
Application NumberANDA091517
ManufacturerBreckenridge Pharmaceutical, Inc.
Substance NameREPAGLINIDE
Strength1
Strength Unitmg/1
Pharmacy ClassesGlinide [EPC], Potassium Channel Antagonists [MoA]

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