NDC 69665-215 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 69665-215 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA204922 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2017-07-01 |
| Marketing End Date | 2019-01-03 |