NDC 68151-2480 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 68151-2480 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA083386 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2017-12-28 |
| Inactivation Date | 2020-01-31 |