NDC 50090-0385 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 50090-0385 |
Marketing Category | / |
Marketing Category | ANDA |
Application Number | ANDA091042 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2014-11-28 |
Marketing End Date | 2018-03-31 |
Marketing Category | ANDA |
Application Number | ANDA091042 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2015-06-09 |
Marketing End Date | 2016-03-31 |
Marketing Category | ANDA |
Application Number | ANDA091042 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2014-11-28 |
Marketing End Date | 2018-03-31 |
Marketing Category | ANDA |
Application Number | ANDA091042 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2015-01-23 |
Marketing End Date | 2016-03-31 |
Marketing Category | ANDA |
Application Number | ANDA091042 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2014-09-10 |
Marketing End Date | 2016-03-31 |