NDC 76147-231 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 76147-231 |
Marketing Category | / |
Marketing Category | OTC monograph not final |
Application Number | part352 |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2019-12-04 |
Marketing End Date | 2019-12-05 |