NDC 0004-0352 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 0004-0352 |
| Marketing Category | / |
| Marketing Category | BLA |
| Application Number | BLA103964 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2002-10-16 |
| Marketing End Date | 2015-07-31 |
| Marketing Category | BLA |
| Application Number | BLA103964 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2011-02-22 |
| Marketing End Date | 2011-08-22 |
| Marketing Category | BLA |
| Application Number | BLA103964 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2002-10-16 |
| Marketing End Date | 2015-07-31 |