NDC 50090-1901 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 50090-1901 |
| Marketing Category | / |
| Marketing Category | NDA AUTHORIZED GENERIC |
| Application Number | NDA019964 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2015-06-25 |
| Marketing End Date | 2016-10-31 |