NDC 60687-248 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 60687-248 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA078703 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2017-02-01 |
| Marketing End Date | 2017-02-22 |
| Marketing Category | ANDA |
| Application Number | ANDA078703 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2017-02-01 |
| Marketing End Date | 2017-02-22 |