NDC 0179-0183 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 0179-0183 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA077095 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2015-07-07 |
| Marketing End Date | 2019-01-31 |