NDC 70518-6430 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 70518-6430 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA076008 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2020-03-30 |
| Marketing End Date | 2020-03-30 |