| NDC Code | 58118-2331-8 |
|---|
| Package Description | 30 TABLET, FILM COATED in 1 BLISTER PACK (58118-2331-8) |
|---|
| Product NDC | 58118-2331 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Glyburide And Metformin Hydrochloride |
|---|
| Non-Proprietary Name | Glyburide And Metformin Hydrochloride |
|---|
| Dosage Form | TABLET, FILM COATED |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20071114 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA077870 |
|---|
| Manufacturer | Clinical Solutions Wholesale |
|---|
| Substance Name | GLYBURIDE; METFORMIN HYDROCHLORIDE |
|---|
| Strength | 2.5; 500 |
|---|
| Strength Unit | mg/1; mg/1 |
|---|
| Pharmacy Classes | Sulfonylurea [EPC],Sulfonylurea Compounds [Chemical/Ingredient],Biguanide [EPC],Biguanides [Chemical/Ingredient] |
|---|