NDC 0004-0820 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 0004-0820 |
| Marketing Category | / |
| Marketing Category | NDA |
| Application Number | NDA021246 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | ML |
| Marketing Start Date | 2011-07-11 |
| Marketing End Date | 2014-09-30 |