NDC 63629-6512 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 63629-6512 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA078216 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2015-07-27 |
| Marketing End Date | 2017-12-30 |