"68001-179-03" National Drug Code (NDC)

Glimepiride 500 TABLET in 1 BOTTLE (68001-179-03)
(BluePoint Laboratories)

NDC Code68001-179-03
Package Description500 TABLET in 1 BOTTLE (68001-179-03)
Product NDC68001-179
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameGlimepiride
Non-Proprietary NameGlimepiride
Dosage FormTABLET
UsageORAL
Start Marketing Date20140226
End Marketing Date20250831
Marketing Category NameANDA
Application NumberANDA078181
ManufacturerBluePoint Laboratories
Substance NameGLIMEPIRIDE
Strength4
Strength Unitmg/1
Pharmacy ClassesSulfonylurea Compounds [CS], Sulfonylurea [EPC]

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