NDC 50814-004 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 50814-004 |
Marketing Category | / |
Marketing Category | OTC monograph not final |
Application Number | part333E |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2016-03-23 |
Marketing End Date | 2016-12-31 |