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Glimepiride - 65862-581-01 - (Glimepiride)

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Drug Information of Glimepiride

Product NDC: 65862-581
Proprietary Name: Glimepiride
Non Proprietary Name: Glimepiride
Active Ingredient(s): 4    mg/1 & nbsp;   Glimepiride
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Glimepiride

Product NDC: 65862-581
Labeler Name: Aurobindo Pharma Limited
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA202759
Marketing Category: ANDA
Start Marketing Date: 20120629

Package Information of Glimepiride

Package NDC: 65862-581-01
Package Description: 100 TABLET in 1 BOTTLE (65862-581-01)

NDC Information of Glimepiride

NDC Code 65862-581-01
Proprietary Name Glimepiride
Package Description 100 TABLET in 1 BOTTLE (65862-581-01)
Product NDC 65862-581
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Glimepiride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20120629
Marketing Category Name ANDA
Labeler Name Aurobindo Pharma Limited
Substance Name GLIMEPIRIDE
Strength Number 4
Strength Unit mg/1
Pharmaceutical Classes Sulfonylurea [EPC],Sulfonylurea Compounds [Chemical/Ingredient]

Complete Information of Glimepiride


General Information