NDC 50090-2136 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 50090-2136 |
Marketing Category | / |
Marketing Category | ANDA |
Application Number | ANDA040581 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2015-10-15 |
Marketing End Date | 2017-09-30 |