NDC 57894-184 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 57894-184 |
| Marketing Category | / |
| Marketing Category | NDA |
| Application Number | NDA202379 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2017-04-17 |
| Marketing End Date | 2017-04-18 |