NDC 50458-605 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 50458-605 |
| Marketing Category | / |
| Marketing Category | NDA |
| Application Number | NDA021444 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2003-04-02 |
| Marketing End Date | 2017-08-31 |