NDC 48792-7898 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 48792-7898 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA208508 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2020-04-09 |
| Marketing End Date | 2020-04-10 |