NDC 70470-1113 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 70470-1113 |
Marketing Category | / |
Marketing Category | OTC monograph final |
Application Number | part346 |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2016-04-01 |
Inactivation Date | 2020-01-31 |