NDC 54868-2185 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 54868-2185 |
| Marketing Category | / |
| Marketing Category | NDA |
| Application Number | NDA019356 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | GM |
| Marketing Start Date | 2005-12-29 |
| Marketing End Date | 2013-03-14 |
| Marketing Category | NDA |
| Application Number | NDA019356 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2013-03-14 |
| Inactivation Date | 2019-09-24 |