NDC 76483-052 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 76483-052 |
| Marketing Category | / |
| Marketing Category | unapproved drug other |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2018-04-10 |
| Inactivation Date | 2020-01-31 |