NDC 60760-142 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 60760-142 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA078332 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2013-04-25 |
| Marketing End Date | 2015-03-31 |
| Marketing Category | ANDA |
| Application Number | ANDA078332 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2013-04-25 |
| Marketing End Date | 2017-01-31 |