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Glimepiride - 61442-117-10 - (Glimepiride)

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Drug Information of Glimepiride

Product NDC: 61442-117
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: 61442-117
Labeler Name: Carlsbad Technology, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077911
Marketing Category: ANDA
Start Marketing Date: 20100201

Package Information of Glimepiride

Package NDC: 61442-117-10
Package Description: 1000 TABLET in 1 BOTTLE (61442-117-10)

NDC Information of Glimepiride

NDC Code 61442-117-10
Proprietary Name Glimepiride
Package Description 1000 TABLET in 1 BOTTLE (61442-117-10)
Product NDC 61442-117
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Glimepiride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20100201
Marketing Category Name ANDA
Labeler Name Carlsbad Technology, Inc.
Substance Name GLIMEPIRIDE
Strength Number 4
Strength Unit mg/1
Pharmaceutical Classes Sulfonylurea [EPC],Sulfonylurea Compounds [Chemical/Ingredient]

Complete Information of Glimepiride


General Information