NDC 70655-143 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 70655-143 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA076766 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | ML |
| Marketing Start Date | 2019-01-31 |
| Marketing End Date | 2018-11-15 |