NDC 63629-5074 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 63629-5074 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA203136 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2013-02-22 |
| Marketing End Date | 2015-02-28 |