NDC 51060-022 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 51060-022 |
Marketing Category | / |
Marketing Category | OTC MONOGRAPH NOT FINAL |
Application Number | part352 |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2014-01-01 |
Marketing End Date | 2017-12-31 |