NDC 0781-2112 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 0781-2112 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA065194 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2004-04-15 |
| Marketing End Date | 2012-04-30 |