NDC 0517-8880 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 0517-8880 |
| Marketing Category | / |
| Marketing Category | NDA |
| Application Number | NDA022382 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2011-04-26 |
| Marketing End Date | 2016-01-14 |
| Marketing Category | NDA |
| Application Number | NDA022382 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2011-04-26 |
| Marketing End Date | 2016-01-14 |