NDC 0781-3122 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 0781-3122 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA078660 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | ML |
| Marketing Start Date | 2012-04-23 |
| Marketing End Date | 2017-11-30 |