NDC 16590-233 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 16590-233 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA064211 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | ML |
| Marketing Start Date | 1998-04-13 |
| Inactivation Date | 2019-10-29 |