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Glimepiride - 0603-3745-28 - (glimepiride)

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Drug Information of Glimepiride

Product NDC: 0603-3745
Proprietary Name: Glimepiride
Non Proprietary Name: glimepiride
Active Ingredient(s): 2    mg/1 & nbsp;   glimepiride
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Glimepiride

Product NDC: 0603-3745
Labeler Name: Qualitest Pharmaceuticals
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077370
Marketing Category: ANDA
Start Marketing Date: 20101014

Package Information of Glimepiride

Package NDC: 0603-3745-28
Package Description: 500 TABLET in 1 BOTTLE, PLASTIC (0603-3745-28)

NDC Information of Glimepiride

NDC Code 0603-3745-28
Proprietary Name Glimepiride
Package Description 500 TABLET in 1 BOTTLE, PLASTIC (0603-3745-28)
Product NDC 0603-3745
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name glimepiride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20101014
Marketing Category Name ANDA
Labeler Name Qualitest Pharmaceuticals
Substance Name GLIMEPIRIDE
Strength Number 2
Strength Unit mg/1
Pharmaceutical Classes Sulfonylurea [EPC],Sulfonylurea Compounds [Chemical/Ingredient]

Complete Information of Glimepiride


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