NDC 0904-5165 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 0904-5165 |
| Marketing Category | / |
| Marketing Category | OTC monograph not final |
| Application Number | part334 |
| Product Type | HUMAN OTC DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2011-05-04 |
| Marketing End Date | 2018-05-31 |