NDC 63629-7801 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 63629-7801 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA064076 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2018-09-19 |
| Marketing End Date | 2018-09-21 |