NDC 0456-2101 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 0456-2101 |
| Marketing Category | / |
| Marketing Category | NDA |
| Application Number | NDA021365 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | ML |
| Marketing Start Date | 2002-11-26 |
| Marketing End Date | 2017-11-30 |