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Glyburide and Metformin - 63629-2793-6 - (Glyburide and Metformin)

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Drug Information of Glyburide and Metformin

Product NDC: 63629-2793
Proprietary Name: Glyburide and Metformin
Non Proprietary Name: Glyburide and Metformin
Active Ingredient(s): 5; 500    mg/1; mg/1 & nbsp;   Glyburide and Metformin
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Glyburide and Metformin

Product NDC: 63629-2793
Labeler Name: Bryant Ranch Prepack
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076345
Marketing Category: ANDA
Start Marketing Date: 20070614

Package Information of Glyburide and Metformin

Package NDC: 63629-2793-6
Package Description: 100 TABLET, FILM COATED in 1 BOTTLE (63629-2793-6)

NDC Information of Glyburide and Metformin

NDC Code 63629-2793-6
Proprietary Name Glyburide and Metformin
Package Description 100 TABLET, FILM COATED in 1 BOTTLE (63629-2793-6)
Product NDC 63629-2793
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Glyburide and Metformin
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20070614
Marketing Category Name ANDA
Labeler Name Bryant Ranch Prepack
Substance Name GLYBURIDE; METFORMIN HYDROCHLORIDE
Strength Number 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


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