NDC 50090-1783 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 50090-1783 |
Marketing Category | / |
Marketing Category | ANDA |
Application Number | ANDA090200 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2015-04-16 |
Marketing End Date | 2016-10-31 |