NDC 60760-229 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 60760-229 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA077091 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2013-05-09 |
| Marketing End Date | 2015-12-31 |
| Marketing Category | ANDA |
| Application Number | ANDA077091 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2013-05-09 |
| Marketing End Date | 2015-10-31 |