NDC Code | 53002-1756-3 |
Package Description | 30 TABLET in 1 BOTTLE (53002-1756-3) |
Product NDC | 53002-1756 |
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 | RPK Pharmaceuticals, Inc. |
Substance Name | PIOGLITAZONE HYDROCHLORIDE |
Strength | 30 |
Strength Unit | mg/1 |
Pharmacy Classes | PPAR alpha [CS], PPAR gamma [CS], Peroxisome Proliferator Receptor alpha Agonist [EPC], Peroxisome Proliferator Receptor gamma Agonist [EPC], Peroxisome Proliferator-activated Receptor Activity [MoA], Thiazolidinedione [EPC], Thiazolidinediones [CS] |