NDC 16590-031 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 16590-031 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA040682 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2007-07-30 |
| Inactivation Date | 2019-10-21 |