NDC 0904-0560 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 0904-0560 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA084903 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2005-04-07 |
| Marketing End Date | 2019-01-11 |