NDC 60505-6206 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 60505-6206 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA078202 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2009-03-30 |
| Marketing End Date | 2009-03-31 |