NDC 0009-5139 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 0009-5139 |
| Marketing Category | / |
| Marketing Category | NDA |
| Application Number | NDA021131 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2000-04-18 |
| Marketing End Date | 2003-07-31 |