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Glimepiride - 0615-6575-39 - (Glimepiride)

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Drug Information of Glimepiride

Product NDC: 0615-6575
Proprietary Name: Glimepiride
Non Proprietary Name: Glimepiride
Active Ingredient(s): 4    mg/1 & nbsp;   Glimepiride
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Glimepiride

Product NDC: 0615-6575
Labeler Name: NCS HealthCare of KY, Inc dba Vangard Labs
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077091
Marketing Category: ANDA
Start Marketing Date: 20051006

Package Information of Glimepiride

Package NDC: 0615-6575-39
Package Description: 30 TABLET, FILM COATED in 1 BLISTER PACK (0615-6575-39)

NDC Information of Glimepiride

NDC Code 0615-6575-39
Proprietary Name Glimepiride
Package Description 30 TABLET, FILM COATED in 1 BLISTER PACK (0615-6575-39)
Product NDC 0615-6575
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Glimepiride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20051006
Marketing Category Name ANDA
Labeler Name NCS HealthCare of KY, Inc dba Vangard Labs
Substance Name GLIMEPIRIDE
Strength Number 4
Strength Unit mg/1
Pharmaceutical Classes Sulfonylurea [EPC],Sulfonylurea Compounds [Chemical/Ingredient]

Complete Information of Glimepiride


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