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 |