NDC 31190-230 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 31190-230 |
Marketing Category | / |
Marketing Category | OTC monograph not final |
Application Number | part352 |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2016-06-25 |
Inactivation Date | 2020-01-31 |
Marketing Category | OTC monograph not final |
Application Number | part352 |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2016-06-25 |
Inactivation Date | 2020-01-31 |