NDC 51239-0912 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 51239-0912 |
Marketing Category | / |
Marketing Category | OTC monograph final |
Application Number | part352 |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2010-03-01 |
Inactivation Date | 2019-10-21 |