| NDC Code | 68788-6888-3 |
|---|
| Package Description | 30 TABLET in 1 BOTTLE (68788-6888-3) |
|---|
| 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] |
|---|