NDC 0409-1212 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 0409-1212 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA070254 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | ML |
| Marketing Start Date | 2005-06-20 |
| Marketing End Date | 2012-01-01 |