NDC 51285-942 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 51285-942 |
| Marketing Category | / |
| Marketing Category | NDA |
| Application Number | NDA021998 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2009-07-28 |
| Marketing End Date | 2016-09-30 |