NDC 49999-739 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 49999-739 |
| Marketing Category | / |
| Marketing Category | NDA |
| Application Number | NDA020592 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2012-03-30 |
| Marketing End Date | 2014-06-01 |