NDC 61924-430 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 61924-430 |
Marketing Category | / |
Marketing Category | OTC monograph final |
Application Number | part347 |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2012-03-02 |
Marketing End Date | 2018-04-05 |