NDC 68788-9099 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 68788-9099 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA040643 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2006-04-26 |
| Marketing End Date | 2013-12-05 |