NDC 40171-003 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 40171-003 |
Marketing Category | / |
Marketing Category | OTC monograph final |
Application Number | part349 |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2008-03-17 |
Marketing End Date | 2017-08-31 |
Marketing Category | OTC monograph final |
Application Number | part349 |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2008-03-17 |
Marketing End Date | 2017-08-31 |