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Glimepiride - 51079-425-20 - (glimepiride)

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Drug Information of Glimepiride

Product NDC: 51079-425
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: 51079-425
Labeler Name: UDL Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077624
Marketing Category: ANDA
Start Marketing Date: 20101104

Package Information of Glimepiride

Package NDC: 51079-425-20
Package Description: 100 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-425-20) > 1 TABLET in 1 BLISTER PACK (51079-425-01)

NDC Information of Glimepiride

NDC Code 51079-425-20
Proprietary Name Glimepiride
Package Description 100 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-425-20) > 1 TABLET in 1 BLISTER PACK (51079-425-01)
Product NDC 51079-425
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 UDL Laboratories, Inc.
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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