NDC 78043-200 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 78043-200 |
Marketing Category | / |
Marketing Category | unapproved drug other |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2020-05-25 |
Marketing End Date | 2020-05-26 |
Marketing Category | unapproved drug other |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2020-05-25 |
Marketing End Date | 2020-05-26 |
Marketing Category | unapproved drug other |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2020-05-25 |
Marketing End Date | 2020-05-26 |
Marketing Category | unapproved drug other |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2020-05-25 |
Marketing End Date | 2020-05-26 |
Marketing Category | unapproved drug other |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2020-05-25 |
Marketing End Date | 2020-05-26 |