NDC 16590-891 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 16590-891 |
Marketing Category | / |
Marketing Category | NDA authorized generic |
Application Number | NDA020406 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2009-11-11 |
Inactivation Date | 2019-11-13 |
Marketing Category | NDA authorized generic |
Application Number | NDA020406 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2009-11-11 |
Inactivation Date | 2019-11-13 |