NDC 63629-7609 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 63629-7609 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA065248 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2018-05-25 |
| Marketing End Date | 2018-05-27 |