Home
>
National Drug Code (NDC)
>
GLUCOVANCE
GLUCOVANCE - 0087-6072-11 - (GLYBURIDE AND METFORMIN HYDROCHLORIDE)
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] |
