NDC 16590-254 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 16590-254 |
| Marketing Category | / |
| Marketing Category | NDA |
| Application Number | NDA021778 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2005-06-08 |
| Inactivation Date | 2019-10-21 |