NDC 54458-883 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 54458-883 |
| Marketing Category | / |
| Marketing Category | NDA AUTHORIZED GENERIC |
| Application Number | NDA021073 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2013-12-08 |
| Marketing End Date | 2017-05-24 |