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Glimepiride - 55154-5070-0 - (glimepiride)

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Drug Information of Glimepiride

Product NDC: 55154-5070
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: 55154-5070
Labeler Name: Cardinal Health
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077624
Marketing Category: ANDA
Start Marketing Date: 20101104

Package Information of Glimepiride

Package NDC: 55154-5070-0
Package Description: 10 BLISTER PACK in 1 BAG (55154-5070-0) > 1 TABLET in 1 BLISTER PACK

NDC Information of Glimepiride

NDC Code 55154-5070-0
Proprietary Name Glimepiride
Package Description 10 BLISTER PACK in 1 BAG (55154-5070-0) > 1 TABLET in 1 BLISTER PACK
Product NDC 55154-5070
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name glimepiride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20101104
Marketing Category Name ANDA
Labeler Name Cardinal Health
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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