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GLYBURIDE AND METFORMIN HYDROCHLORIDE - 55111-696-05 - (GLYBURIDE AND METFORMIN HYDROCHLORIDE)

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Drug Information of GLYBURIDE AND METFORMIN HYDROCHLORIDE

Product NDC: 55111-696
Proprietary Name: GLYBURIDE AND METFORMIN HYDROCHLORIDE
Non Proprietary Name: GLYBURIDE AND METFORMIN HYDROCHLORIDE
Active Ingredient(s): 2.5; 500    mg/1; mg/1 & nbsp;   GLYBURIDE AND METFORMIN HYDROCHLORIDE
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of GLYBURIDE AND METFORMIN HYDROCHLORIDE

Product NDC: 55111-696
Labeler Name: Dr. Reddy's Laboratories Limited
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA079009
Marketing Category: ANDA
Start Marketing Date: 20090630

Package Information of GLYBURIDE AND METFORMIN HYDROCHLORIDE

Package NDC: 55111-696-05
Package Description: 500 TABLET in 1 BOTTLE (55111-696-05)

NDC Information of GLYBURIDE AND METFORMIN HYDROCHLORIDE

NDC Code 55111-696-05
Proprietary Name GLYBURIDE AND METFORMIN HYDROCHLORIDE
Package Description 500 TABLET in 1 BOTTLE (55111-696-05)
Product NDC 55111-696
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name GLYBURIDE AND METFORMIN HYDROCHLORIDE
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20090630
Marketing Category Name ANDA
Labeler Name Dr. Reddy's Laboratories Limited
Substance Name GLYBURIDE; METFORMIN HYDROCHLORIDE
Strength Number 2.5; 500
Strength Unit mg/1; mg/1
Pharmaceutical Classes Sulfonylurea [EPC],Sulfonylurea Compounds [Chemical/Ingredient],Biguanide [EPC],Biguanides [Chemical/Ingredient]

Complete Information of GLYBURIDE AND METFORMIN HYDROCHLORIDE


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