NDC 54868-2470 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 54868-2470 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA063305 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | GM |
| Marketing Start Date | 2005-03-03 |
| Inactivation Date | 2019-09-24 |