NDC 16590-064 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 16590-064 |
| Marketing Category | / |
| Marketing Category | NDA |
| Application Number | NDA020685 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 1996-03-13 |
| Inactivation Date | 2019-11-13 |