NDC 0517-0795 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 0517-0795 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA091329 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2011-04-08 |
| Marketing End Date | 2011-04-08 |
| Inactivation Date | 2019-10-29 |
| Reactivation Date | 2020-04-13 |