NDC 0409-4778 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 0409-4778 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA077245 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | ML |
| Marketing Start Date | 2006-08-28 |
| Marketing End Date | 2015-11-01 |