NDC 50090-1072 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 50090-1072 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA078787 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2014-11-28 |
| Marketing End Date | 2017-08-31 |