NDC 0591-3768 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 0591-3768 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA078404 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | ML |
| Marketing Start Date | 2015-02-17 |
| Marketing End Date | 2018-05-31 |