| NDC Code | 51991-709-90 |
|---|
| Package Description | 90 TABLET in 1 BOTTLE (51991-709-90) |
|---|
| Product NDC | 51991-709 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Pioglitazone Hydrochloride |
|---|
| Non-Proprietary Name | Pioglitazone Hydrochloride |
|---|
| Dosage Form | TABLET |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20130213 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA078472 |
|---|
| Manufacturer | Breckenridge Pharmaceutical, Inc. |
|---|
| Substance Name | PIOGLITAZONE HYDROCHLORIDE |
|---|
| Strength | 30 |
|---|
| 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] |
|---|