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Glimepiride - 54868-3377-0 - (Glimepiride)

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Drug Information of Glimepiride

Product NDC: 54868-3377
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: 54868-3377
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076802
Marketing Category: ANDA
Start Marketing Date: 20051019

Package Information of Glimepiride

Package NDC: 54868-3377-0
Package Description: 30 TABLET in 1 BOTTLE (54868-3377-0)

NDC Information of Glimepiride

NDC Code 54868-3377-0
Proprietary Name Glimepiride
Package Description 30 TABLET in 1 BOTTLE (54868-3377-0)
Product NDC 54868-3377
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Glimepiride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20051019
Marketing Category Name ANDA
Labeler Name Physicians Total Care, 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