NDC 0004-0380 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 0004-0380 |
| Marketing Category | / |
| Marketing Category | NDA |
| Application Number | NDA021481 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2003-03-13 |
| Marketing End Date | 2013-06-30 |