NDC 50458-170 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 50458-170 |
| Marketing Category | / |
| Marketing Category | NDA |
| Application Number | NDA021721 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | ML |
| Marketing Start Date | 2004-10-21 |
| Marketing End Date | 2015-04-30 |