| NDC Code | 65862-081-05 |
|---|
| Package Description | 500 TABLET, FILM COATED in 1 BOTTLE (65862-081-05) |
|---|
| Product NDC | 65862-081 |
|---|
| 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 | Aurobindo Pharma Limited |
|---|
| Substance Name | GLYBURIDE; METFORMIN HYDROCHLORIDE |
|---|
| Strength | 2.5; 500 |
|---|
| Strength Unit | mg/1; mg/1 |
|---|
| Pharmacy Classes | Biguanide [EPC], Biguanides [CS], Sulfonylurea Compounds [CS], Sulfonylurea [EPC] |
|---|