NDC 54868-3777 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 54868-3777 |
| Marketing Category | / |
| Marketing Category | NDA |
| Application Number | NDA020132 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 1996-06-10 |
| Marketing End Date | 2011-06-30 |