NDC 50458-164 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 50458-164 |
| Marketing Category | / |
| Marketing Category | NDA |
| Application Number | NDA020635 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 1996-12-20 |
| Marketing End Date | 2014-07-09 |