NDC 68453-912 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 68453-912 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA040658 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2007-06-05 |
| Marketing End Date | 2013-05-12 |