NDC 68084-526 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 68084-526 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA076255 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2012-04-25 |
| Marketing End Date | 2015-09-30 |
| Marketing Category | ANDA |
| Application Number | ANDA076255 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2012-04-25 |
| Marketing End Date | 2015-09-30 |