NDC 49401-104 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 49401-104 |
| Marketing Category | / |
| Marketing Category | BLA |
| Application Number | BLA125349 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2012-12-14 |
| Marketing End Date | 2018-08-13 |