GLUCOVANCE - 0087-6072-11 - (GLYBURIDE AND METFORMIN HYDROCHLORIDE)

Alphabetical Index


Drug Information of GLUCOVANCE

Product NDC: 0087-6072
Proprietary Name: GLUCOVANCE
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 GLUCOVANCE

Product NDC: 0087-6072
Labeler Name: Bristol-Myers Squibb Company
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021178
Marketing Category: NDA
Start Marketing Date: 20081215

Package Information of GLUCOVANCE

Package NDC: 0087-6072-11
Package Description: 100 TABLET, FILM COATED in 1 BOTTLE (0087-6072-11)

NDC Information of GLUCOVANCE

NDC Code 0087-6072-11
Proprietary Name GLUCOVANCE
Package Description 100 TABLET, FILM COATED in 1 BOTTLE (0087-6072-11)
Product NDC 0087-6072
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 20081215
Marketing Category Name NDA
Labeler Name Bristol-Myers Squibb Company
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 GLUCOVANCE


General Information