NDC 70655-015 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 70655-015 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA210231 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2018-08-29 |
| Marketing End Date | 2019-06-28 |
| Marketing Category | ANDA |
| Application Number | ANDA210231 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2019-06-28 |
| Marketing End Date | 2019-06-28 |