NDC 60505-2638 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 60505-2638 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA078389 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2008-05-16 |
| Marketing End Date | 2009-04-20 |
| Marketing Category | ANDA |
| Application Number | ANDA078389 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2008-05-16 |
| Marketing End Date | 2009-04-20 |
| Marketing Category | ANDA |
| Application Number | ANDA078389 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2008-05-16 |
| Marketing End Date | 2009-04-20 |
| Marketing Category | ANDA |
| Application Number | ANDA078389 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2008-05-16 |
| Marketing End Date | 2009-04-20 |