NDC 60505-2504 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 60505-2504 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA076795 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2004-11-29 |
| Marketing End Date | 2010-11-30 |
| Marketing Category | ANDA |
| Application Number | ANDA076795 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2004-11-29 |
| Marketing End Date | 2010-11-30 |
| Marketing Category | ANDA |
| Application Number | ANDA076795 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2004-11-29 |
| Marketing End Date | 2010-11-30 |