NDC 52544-475 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 52544-475 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA078666 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2009-07-21 |
| Marketing End Date | 2011-04-30 |