NDC 16590-278 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 16590-278 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA040114 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 1996-03-14 |
| Inactivation Date | 2019-11-13 |