NDC 0078-0339 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 0078-0339 |
| Marketing Category | / |
| Marketing Category | NDA |
| Application Number | NDA021025 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | ML |
| Marketing Start Date | 2000-04-30 |
| Marketing End Date | 2014-06-30 |