"42571-105-10" National Drug Code (NDC)

Glimepiride 1000 TABLET in 1 BOTTLE (42571-105-10)
(Micro Labs Limited)

NDC Code42571-105-10
Package Description1000 TABLET in 1 BOTTLE (42571-105-10)
Product NDC42571-105
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
Strength8
Strength Unitmg/1
Pharmacy ClassesSulfonylurea [EPC],Sulfonylurea Compounds [Chemical/Ingredient]

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