NDC 16590-539 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 16590-539 |
Marketing Category | / |
Marketing Category | ANDA |
Application Number | ANDA077634 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2006-03-17 |
Inactivation Date | 2019-11-13 |
Marketing Category | ANDA |
Application Number | ANDA077634 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2006-03-17 |
Inactivation Date | 2019-11-13 |
Marketing Category | ANDA |
Application Number | ANDA077634 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2006-03-17 |
Inactivation Date | 2019-11-13 |
Marketing Category | ANDA |
Application Number | ANDA077634 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2006-03-17 |
Inactivation Date | 2019-11-13 |