NDC Code | 68084-615-01 |
Package Description | 10 BLISTER PACK in 1 CARTON (68084-615-01) > 10 TABLET in 1 BLISTER PACK (68084-615-11) |
Product NDC | 68084-615 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Proprietary Name | Pioglitazone Hydrochloride |
Non-Proprietary Name | Pioglitazone Hydrochloride |
Dosage Form | TABLET |
Usage | ORAL |
Start Marketing Date | 20130620 |
Marketing Category Name | ANDA |
Application Number | ANDA200268 |
Manufacturer | American Health Packaging |
Substance Name | PIOGLITAZONE HYDROCHLORIDE |
Strength | 45 |
Strength Unit | mg/1 |
Pharmacy Classes | Peroxisome Proliferator Receptor alpha Agonist [EPC],Peroxisome Proliferator Receptor gamma Agonist [EPC],Peroxisome Proliferator-activated Receptor Activity [MoA],PPAR alpha [Chemical/Ingredient],PPAR gamma [Chemical/Ingredient],Thiazolidinedione [EPC],Thiazolidinediones [Chemical/Ingredient] |