NDC 63629-6477 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 63629-6477 |
| Marketing Category | / |
| Marketing Category | NDA AUTHORIZED GENERIC |
| Application Number | NDA021283 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2015-09-04 |
| Marketing End Date | 2017-05-30 |