NDC 55390-062 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 55390-062 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA076323 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | ML |
| Marketing Start Date | 2004-10-04 |
| Marketing End Date | 2014-09-30 |