NDC 69512-020 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 69512-020 |
| Marketing Category | / |
| Marketing Category | unapproved drug other |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2015-03-15 |
| Inactivation Date | 2020-01-31 |