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Glimepiride - 21695-747-60 - (Glimepiride)

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Drug Information of Glimepiride

Product NDC: 21695-747
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: 21695-747
Labeler Name: Rebel Distributors Corp
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077091
Marketing Category: ANDA
Start Marketing Date: 20051006

Package Information of Glimepiride

Package NDC: 21695-747-60
Package Description: 60 TABLET in 1 BOTTLE (21695-747-60)

NDC Information of Glimepiride

NDC Code 21695-747-60
Proprietary Name Glimepiride
Package Description 60 TABLET in 1 BOTTLE (21695-747-60)
Product NDC 21695-747
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Glimepiride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20051006
Marketing Category Name ANDA
Labeler Name Rebel Distributors Corp
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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