NDC 59572-983 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 59572-983 |
| Marketing Category | / |
| Marketing Category | NDA |
| Application Number | NDA022393 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2010-01-04 |
| Marketing End Date | 2016-07-27 |