NDC 0004-0810 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 0004-0810 |
| Marketing Category | / |
| Marketing Category | NDA |
| Application Number | NDA021246 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2000-12-14 |
| Marketing End Date | 2012-09-04 |