NDC 16590-368 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 16590-368 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA073030 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 1994-10-17 |
| Inactivation Date | 2019-10-21 |