NDC 16590-461 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 16590-461 |
| Marketing Category | / |
| Marketing Category | NDA |
| Application Number | NDA020864 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 1998-06-29 |
| Inactivation Date | 2019-10-29 |