NDC 60760-356 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 60760-356 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA090548 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2016-04-20 |
| Marketing End Date | 2016-11-30 |