NDC 0179-0219 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 0179-0219 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA076052 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2016-09-28 |
| Marketing End Date | 2018-07-31 |