NDC 0378-6015 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 0378-6015 |
| Marketing Category | / |
| Marketing Category | NDA |
| Application Number | NDA020897 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2007-05-10 |
| Marketing End Date | 2016-07-30 |