NDC 68547-002 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 68547-002 |
| Marketing Category | / |
| Marketing Category | NDA |
| Application Number | NDA209360 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2020-03-12 |
| Marketing End Date | 2018-02-07 |