NDC 75021-001 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 75021-001 |
Marketing Category | / |
Marketing Category | OTC monograph not final |
Application Number | part333A |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2020-04-10 |
Marketing End Date | 2020-04-12 |