NDC 63629-7248 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 63629-7248 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA077270 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2017-04-17 |
| Marketing End Date | 2017-11-30 |