NDC 68788-7157 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 68788-7157 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA078295 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2018-06-01 |
| Marketing End Date | 2018-06-05 |