NDC Code | 68788-6888-6 |
Package Description | 60 TABLET in 1 BOTTLE (68788-6888-6) |
Product NDC | 68788-6888 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Proprietary Name | Pioglitazone Hydrochloride |
Non-Proprietary Name | Pioglitazone Hydrochloride |
Dosage Form | TABLET |
Usage | ORAL |
Start Marketing Date | 20170201 |
Marketing Category Name | ANDA |
Application Number | ANDA200044 |
Manufacturer | Preferred Pharmaceuticals Inc. |
Substance Name | PIOGLITAZONE HYDROCHLORIDE |
Strength | 45 |
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] |