NDC 54868-3835 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 54868-3835 |
| Marketing Category | / |
| Marketing Category | NDA |
| Application Number | NDA020136 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2000-11-28 |
| Inactivation Date | 2019-09-24 |