| NDC Code | 70882-105-56 |
|---|
| Package Description | 56 TABLET, FILM COATED in 1 BLISTER PACK (70882-105-56) |
|---|
| Product NDC | 70882-105 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Pioglitazone And Metformin |
|---|
| Non-Proprietary Name | Pioglitazone And Metformin |
|---|
| Dosage Form | TABLET, FILM COATED |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20130502 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA091273 |
|---|
| Manufacturer | Cambridge Therapeutics Technologies, LLC |
|---|
| Substance Name | PIOGLITAZONE HYDROCHLORIDE; METFORMIN HYDROCHLORIDE |
|---|
| Strength | 15; 500 |
|---|
| Strength Unit | mg/1; mg/1 |
|---|
| Pharmacy Classes | Peroxisome Proliferator-activated Receptor Activity [MoA],PPAR alpha [CS],PPAR gamma [CS],Thiazolidinedione [EPC],Thiazolidinediones [CS],Peroxisome Proliferator Receptor alpha Agonist [EPC],Peroxisome Proliferator Receptor gamma Agonist [EPC],Biguanide [EPC],Biguanides [CS] |
|---|