NDC 63739-388 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 63739-388 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA075718 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2007-08-06 |
| Marketing End Date | 2010-11-01 |