NDC 36800-912 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 36800-912 |
Marketing Category | / |
Marketing Category | OTC monograph final |
Application Number | part341 |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2007-08-06 |
Marketing End Date | 2014-09-18 |