| Product NDC: | 64764-451 |
| Proprietary Name: | Actos |
| Non Proprietary Name: | pioglitazone |
| Active Ingredient(s): | 45 mg/1 & nbsp; pioglitazone |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 64764-451 |
| Labeler Name: | Takeda Pharmaceuticals America, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA021073 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19990715 |
| Package NDC: | 64764-451-24 |
| Package Description: | 30 TABLET in 1 BOTTLE (64764-451-24) |
| NDC Code | 64764-451-24 |
| Proprietary Name | Actos |
| Package Description | 30 TABLET in 1 BOTTLE (64764-451-24) |
| Product NDC | 64764-451 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | pioglitazone |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 19990715 |
| Marketing Category Name | NDA |
| Labeler Name | Takeda Pharmaceuticals America, Inc. |
| Substance Name | PIOGLITAZONE HYDROCHLORIDE |
| Strength Number | 45 |
| Strength Unit | mg/1 |
| Pharmaceutical 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] |