| NDC Code | 23155-233-05 |
|---|
| Package Description | 500 TABLET in 1 BOTTLE (23155-233-05) |
|---|
| Product NDC | 23155-233 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Glyburide-metformin Hydrochloride |
|---|
| Non-Proprietary Name | Glyburide-metformin Hydrochloride |
|---|
| Dosage Form | TABLET |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20240501 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA079009 |
|---|
| Manufacturer | Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc. |
|---|
| Substance Name | GLYBURIDE; METFORMIN HYDROCHLORIDE |
|---|
| Strength | 1.25; 250 |
|---|
| Strength Unit | mg/1; mg/1 |
|---|
| Pharmacy Classes | Biguanide [EPC], Biguanides [CS], Sulfonylurea Compounds [CS], Sulfonylurea [EPC] |
|---|