NDC 0406-0362 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 0406-0362 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA040084 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2010-04-22 |
| Marketing End Date | 2016-06-30 |