| NDC Code | 68382-186-16 |
|---|
| Package Description | 90 TABLET, FILM COATED in 1 BOTTLE (68382-186-16) |
|---|
| Product NDC | 68382-186 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Glipizide And Metformin Hydrochloride |
|---|
| Non-Proprietary Name | Glipizide And Metformin Hydrochloride |
|---|
| Dosage Form | TABLET, FILM COATED |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20160505 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA078905 |
|---|
| Manufacturer | Zydus Pharmaceuticals USA Inc. |
|---|
| Substance Name | GLIPIZIDE; METFORMIN HYDROCHLORIDE |
|---|
| Strength | 5; 500 |
|---|
| Strength Unit | mg/1; mg/1 |
|---|
| Pharmacy Classes | Biguanide [EPC], Biguanides [CS], Sulfonylurea Compounds [CS], Sulfonylurea [EPC] |
|---|