NDC 60505-2520 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 60505-2520 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA077046 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2011-08-01 |
| Marketing End Date | 2016-08-01 |
| Marketing Category | ANDA |
| Application Number | ANDA077046 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2011-08-01 |
| Marketing End Date | 2016-08-01 |
| Marketing Category | ANDA |
| Application Number | ANDA077046 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2011-08-01 |
| Marketing End Date | 2016-08-01 |
| Marketing Category | ANDA |
| Application Number | ANDA077046 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2011-08-01 |
| Marketing End Date | 2016-08-01 |