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Glimepiride - 55111-320-78 - (Glimepiride)

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Drug Information of Glimepiride

Product NDC: 55111-320
Proprietary Name: Glimepiride
Non Proprietary Name: Glimepiride
Active Ingredient(s): 1    mg/1 & nbsp;   Glimepiride
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Glimepiride

Product NDC: 55111-320
Labeler Name: Dr. Reddy's Laboratories Limited
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077091
Marketing Category: ANDA
Start Marketing Date: 20051006

Package Information of Glimepiride

Package NDC: 55111-320-78
Package Description: 10 BLISTER PACK in 1 CARTON (55111-320-78) > 10 TABLET in 1 BLISTER PACK

NDC Information of Glimepiride

NDC Code 55111-320-78
Proprietary Name Glimepiride
Package Description 10 BLISTER PACK in 1 CARTON (55111-320-78) > 10 TABLET in 1 BLISTER PACK
Product NDC 55111-320
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 Dr. Reddy's Laboratories Limited
Substance Name GLIMEPIRIDE
Strength Number 1
Strength Unit mg/1
Pharmaceutical Classes Sulfonylurea [EPC],Sulfonylurea Compounds [Chemical/Ingredient]

Complete Information of Glimepiride


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