NDC 0603-4022 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 0603-4022 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA078558 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2009-11-23 |
| Marketing End Date | 2013-01-01 |
| Marketing Category | ANDA |
| Application Number | ANDA078558 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2009-11-23 |
| Marketing End Date | 2013-01-01 |