NDC 16590-421 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 16590-421 |
| Marketing Category | / |
| Marketing Category | NDA authorized generic |
| Application Number | NDA019992 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | ML |
| Marketing Start Date | 2004-05-07 |
| Inactivation Date | 2019-11-27 |