NDC 60505-6088 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 60505-6088 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA065231 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2005-08-02 |
| Marketing End Date | 2020-04-07 |