NDC 24987-562 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 24987-562 |
| Marketing Category | / |
| Marketing Category | NDA |
| Application Number | NDA009768 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2013-06-28 |
| Marketing End Date | 2017-12-31 |
| Marketing Category | NDA |
| Application Number | NDA009768 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2013-06-28 |
| Marketing End Date | 2016-09-30 |