NDC 70655-078 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 70655-078 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA210989 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2019-12-31 |
| Marketing End Date | 2019-12-31 |
| Marketing Category | ANDA |
| Application Number | ANDA210989 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2019-12-31 |
| Marketing End Date | 2019-12-31 |
| Marketing Category | ANDA |
| Application Number | ANDA210989 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2019-12-31 |
| Marketing End Date | 2019-12-31 |