NDC 16590-878 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 16590-878 |
Marketing Category | / |
Marketing Category | ANDA |
Application Number | ANDA076642 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2008-12-16 |
Inactivation Date | 2019-10-21 |
Marketing Category | ANDA |
Application Number | ANDA076642 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2008-12-16 |
Inactivation Date | 2019-10-21 |
Marketing Category | ANDA |
Application Number | ANDA076642 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2008-12-16 |
Inactivation Date | 2019-10-21 |