"52125-389-23" National Drug Code (NDC)

Glimepiride 180 TABLET in 1 BOTTLE (52125-389-23)
(REMEDYREPACK INC.)

NDC Code52125-389-23
Package Description180 TABLET in 1 BOTTLE (52125-389-23)
Product NDC52125-389
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameGlimepiride
Non-Proprietary NameGlimepiride
Dosage FormTABLET
UsageORAL
Start Marketing Date20150722
Marketing Category NameANDA
Application NumberANDA077091
ManufacturerREMEDYREPACK INC.
Substance NameGLIMEPIRIDE
Strength4
Strength Unitmg/1
Pharmacy ClassesSulfonylurea [EPC],Sulfonylurea Compounds [Chemical/Ingredient]

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