NDC 69379-041 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 69379-041 |
Marketing Category | / |
Marketing Category | OTC monograph not final |
Application Number | part348 |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2015-07-01 |
Marketing End Date | 2015-07-13 |