NDC 50090-2112 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 50090-2112 |
Marketing Category | / |
Marketing Category | NDA authorized generic |
Application Number | NDA021656 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2015-10-14 |
Marketing End Date | 2018-10-31 |