NDC 54868-6274 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 54868-6274 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA076629 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2011-06-21 |
| Inactivation Date | 2019-09-24 |