NDC 67386-521 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 67386-521 | 
| Marketing Category | / | 
| Marketing Category | BLA | 
| Application Number | BLA125284 | 
| Product Type | HUMAN PRESCRIPTION DRUG | 
| Billing Unit | EA | 
| Marketing Start Date | 2009-02-06 |