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Glyburide and Metformin Hydrochloride - 0093-5710-83 - (Glyburide and Metformin Hydrochloride)

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Drug Information of Glyburide and Metformin Hydrochloride

Product NDC: 0093-5710
Proprietary Name: Glyburide and Metformin Hydrochloride
Non Proprietary Name: Glyburide and Metformin Hydrochloride
Active Ingredient(s): 1.25; 250    mg/1; mg/1 & nbsp;   Glyburide and Metformin Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Glyburide and Metformin Hydrochloride

Product NDC: 0093-5710
Labeler Name: Teva Pharmaceuticals USA Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076345
Marketing Category: ANDA
Start Marketing Date: 20070614

Package Information of Glyburide and Metformin Hydrochloride

Package NDC: 0093-5710-83
Package Description: 3000 TABLET, FILM COATED in 1 BOTTLE (0093-5710-83)

NDC Information of Glyburide and Metformin Hydrochloride

NDC Code 0093-5710-83
Proprietary Name Glyburide and Metformin Hydrochloride
Package Description 3000 TABLET, FILM COATED in 1 BOTTLE (0093-5710-83)
Product NDC 0093-5710
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Glyburide and Metformin Hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20070614
Marketing Category Name ANDA
Labeler Name Teva Pharmaceuticals USA Inc
Substance Name GLYBURIDE; METFORMIN HYDROCHLORIDE
Strength Number 1.25; 250
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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