| NDC Code | 82009-105-05 |
|---|
| Package Description | 500 TABLET in 1 BOTTLE (82009-105-05) |
|---|
| Product NDC | 82009-105 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Pioglitazone Hydrochloride |
|---|
| Non-Proprietary Name | Pioglitazone Hydrochloride |
|---|
| Dosage Form | TABLET |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20230801 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA200268 |
|---|
| Manufacturer | QUALLENT PHARMACEUTICALS HEALTH LLC |
|---|
| 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 alpha Agonists [MoA], Peroxisome Proliferator-activated Receptor gamma Agonists [MoA], Thiazolidinedione [EPC], Thiazolidinediones [CS] |
|---|