NDC 50090-1002 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 50090-1002 |
Marketing Category | / |
Marketing Category | ANDA |
Application Number | ANDA040256 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2014-11-28 |
Marketing End Date | 2019-07-31 |