NDC 0007-4515 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 0007-4515 |
| Marketing Category | / |
| Marketing Category | NDA |
| Application Number | NDA022291 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2016-11-27 |
| Marketing End Date | 2016-11-28 |