NDC 70518-6460 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 70518-6460 |
| Marketing Category | / |
| Marketing Category | NDA authorized generic |
| Application Number | NDA022047 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2020-03-30 |
| Marketing End Date | 2020-03-30 |