NDC 0004-0360 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 0004-0360 |
Marketing Category | / |
Marketing Category | BLA |
Application Number | BLA103964 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2011-11-01 |
Marketing End Date | 2018-02-08 |
Marketing Category | BLA |
Application Number | BLA103964 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | ML |
Marketing Start Date | 2011-11-01 |
Marketing End Date | 2019-01-31 |