NDC 0430-0477 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 0430-0477 |
| Marketing Category | / |
| Marketing Category | NDA |
| Application Number | NDA020835 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2007-04-16 |
| Marketing End Date | 2010-03-31 |