NDC 59630-762 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 59630-762 |
| Marketing Category | / |
| Marketing Category | NDA |
| Application Number | NDA021475 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2010-11-01 |
| Marketing End Date | 2014-01-01 |