NDC 50814-003 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 50814-003 |
| Marketing Category | / |
| Marketing Category | OTC monograph final |
| Application Number | part333B |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2016-03-23 |
| Marketing End Date | 2016-12-08 |