NDC 11673-722 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 11673-722 |
Marketing Category | / |
Marketing Category | OTC monograph final |
Application Number | part331 |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2013-03-08 |
Marketing End Date | 2018-06-30 |