NDC 62372-700 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 62372-700 |
Marketing Category | / |
Marketing Category | OTC monograph final |
Application Number | part341 |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2014-06-01 |
Marketing End Date | 2017-03-31 |