NDC 69512-030 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 69512-030 |
| Marketing Category | / |
| Marketing Category | unapproved drug other |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | GM |
| Marketing Start Date | 2015-03-01 |
| Marketing End Date | 2015-06-08 |