NDC 68151-2049 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 68151-2049 |
| Marketing Category | / |
| Marketing Category | NDA AUTHORIZED GENERIC |
| Application Number | NDA021228 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2016-06-16 |
| Marketing End Date | 2016-06-17 |