NDC 0185-0204 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 0185-0204 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA076631 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2004-02-11 |
| Marketing End Date | 2015-09-30 |