NDC 67296-0105 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 67296-0105 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA075738 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2009-06-08 |
| Inactivation Date | 2019-10-29 |