NDC 50090-2114 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 50090-2114 |
| Marketing Category | / |
| Marketing Category | NDA authorized generic |
| Application Number | NDA018279 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2015-10-14 |
| Marketing End Date | 2017-12-31 |
| Marketing Category | NDA authorized generic |
| Application Number | NDA018279 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2015-10-14 |
| Marketing End Date | 2017-12-31 |