NDC Code | 0378-1550-91 |
Package Description | 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-1550-91) |
Product NDC | 0378-1550 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Proprietary Name | Pioglitazone Hydrochloride And Metformin Hydrochloride |
Non-Proprietary Name | Pioglitazone Hydrochloride And Metformin Hydrochloride |
Dosage Form | TABLET, FILM COATED |
Usage | ORAL |
Start Marketing Date | 20120817 |
End Marketing Date | 20190630 |
Marketing Category Name | ANDA |
Application Number | ANDA090406 |
Manufacturer | Mylan Pharmaceuticals Inc. |
Substance Name | PIOGLITAZONE HYDROCHLORIDE; METFORMIN HYDROCHLORIDE |
Strength | 15; 500 |
Strength Unit | mg/1; mg/1 |
Pharmacy Classes | Peroxisome Proliferator-activated Receptor Activity [MoA],PPAR alpha [CS],PPAR gamma [CS],Thiazolidinedione [EPC],Thiazolidinediones [CS],Peroxisome Proliferator Receptor alpha Agonist [EPC],Peroxisome Proliferator Receptor gamma Agonist [EPC],Biguanide [EPC],Biguanides [CS] |