NDC 51645-717 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 51645-717 |
| Marketing Category | / |
| Marketing Category | OTC monograph not final |
| Application Number | part343 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2013-01-10 |
| Marketing End Date | 2017-11-30 |