NDC 0406-8886 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 0406-8886 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA040440 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2010-02-18 |
| Marketing End Date | 2017-05-31 |