"42571-101-05" National Drug Code (NDC)

Glimepiride 500 TABLET in 1 BOTTLE (42571-101-05)
(Micro Labs Limited)

NDC Code42571-101-05
Package Description500 TABLET in 1 BOTTLE (42571-101-05)
Product NDC42571-101
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameGlimepiride
Non-Proprietary NameGlimepiride
Dosage FormTABLET
UsageORAL
Start Marketing Date20130613
Marketing Category NameANDA
Application NumberANDA091220
ManufacturerMicro Labs Limited
Substance NameGLIMEPIRIDE
Strength2
Strength Unitmg/1
Pharmacy ClassesSulfonylurea Compounds [CS], Sulfonylurea [EPC]

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