NDC 0281-7062 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 0281-7062 |
| Marketing Category | / |
| Marketing Category | NDA |
| Application Number | NDA009190 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2007-02-28 |
| Marketing End Date | 2016-09-30 |