NDC 60505-2638 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 60505-2638 |
Marketing Category | / |
Marketing Category | ANDA |
Application Number | ANDA078389 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2008-05-16 |
Marketing End Date | 2009-04-20 |
Marketing Category | ANDA |
Application Number | ANDA078389 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2008-05-16 |
Marketing End Date | 2009-04-20 |
Marketing Category | ANDA |
Application Number | ANDA078389 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2008-05-16 |
Marketing End Date | 2009-04-20 |
Marketing Category | ANDA |
Application Number | ANDA078389 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2008-05-16 |
Marketing End Date | 2009-04-20 |