NDC 45802-822 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 45802-822 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA077295 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2005-10-06 |
| Marketing End Date | 2015-10-01 |