| NDC Code | 68180-490-01 |
|---|
| Package Description | 100 TABLET in 1 BOTTLE (68180-490-01) |
|---|
| Product NDC | 68180-490 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Repaglinide And Metformin Hydrochloride |
|---|
| Non-Proprietary Name | Repaglinide And Metformin Hydrochloride |
|---|
| Dosage Form | TABLET |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20151210 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA200624 |
|---|
| Manufacturer | Lupin Pharmaceuticals, Inc. |
|---|
| Substance Name | METFORMIN HYDROCHLORIDE; REPAGLINIDE |
|---|
| Strength | 500; 1 |
|---|
| Strength Unit | mg/1; mg/1 |
|---|
| Pharmacy Classes | Biguanide [EPC],Biguanides [CS],Glinide [EPC],Potassium Channel Antagonists [MoA] |
|---|