NDC Code | 33342-176-57 |
Package Description | 180 TABLET in 1 BOTTLE (33342-176-57) |
Product NDC | 33342-176 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Proprietary Name | Pioglitazole And Metformin Hydrochloride |
Non-Proprietary Name | Pioglitazole And Metformin Hydrochloride |
Dosage Form | TABLET |
Usage | ORAL |
Start Marketing Date | 20151106 |
Marketing Category Name | ANDA |
Application Number | ANDA204802 |
Manufacturer | Macleods Pharmaceuticals Limited |
Substance Name | METFORMIN HYDROCHLORIDE; PIOGLITAZONE HYDROCHLORIDE |
Strength | 500; 15 |
Strength Unit | mg/1; mg/1 |
Pharmacy Classes | Biguanide [EPC], Biguanides [CS], Peroxisome Proliferator Receptor alpha Agonist [EPC], Peroxisome Proliferator Receptor gamma Agonist [EPC], Peroxisome Proliferator-activated Receptor alpha Agonists [MoA], Peroxisome Proliferator-activated Receptor gamma Agonists [MoA], Thiazolidinedione [EPC], Thiazolidinediones [CS] |