NDC 59011-522 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 59011-522 |
| Marketing Category | / |
| Marketing Category | NDA |
| Application Number | NDA205777 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2020-01-01 |
| Inactivation Date | 2020-01-31 |