NDC 64720-322 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 64720-322 |
| Marketing Category | / |
| Marketing Category | NDA |
| Application Number | NDA020859 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2008-05-01 |
| Marketing End Date | 2014-05-01 |