NDC 0185-0221 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 0185-0221 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA075965 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2002-01-25 |
| Marketing End Date | 2007-12-31 |
| Marketing Category | ANDA |
| Application Number | ANDA075965 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2002-01-25 |
| Marketing End Date | 2007-05-31 |