NDC 54766-732 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 54766-732 |
| Marketing Category | / |
| Marketing Category | unapproved drug other |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2015-08-07 |
| Marketing End Date | 2017-02-28 |