NDC Code | 13668-140-53 |
Package Description | 9000 TABLET in 1 BOTTLE (13668-140-53) |
Product NDC | 13668-140 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Proprietary Name | Pioglitazonehydrochloride |
Non-Proprietary Name | Pioglitazonehydrochloride |
Dosage Form | TABLET |
Usage | ORAL |
Start Marketing Date | 20130213 |
Marketing Category Name | ANDA |
Application Number | ANDA091298 |
Manufacturer | Torrent Pharmaceuticals Limited |
Substance Name | PIOGLITAZONE HYDROCHLORIDE |
Strength | 15 |
Strength Unit | 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] |