NDC 76631-005 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 76631-005 |
Marketing Category | / |
Marketing Category | unapproved drug other |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2020-04-29 |
Marketing End Date | 2020-04-30 |
Marketing Category | unapproved drug other |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2020-04-29 |
Marketing End Date | 2020-04-30 |
Marketing Category | unapproved drug other |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2020-04-29 |
Marketing End Date | 2020-04-30 |
Marketing Category | unapproved drug other |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2020-04-29 |
Marketing End Date | 2020-04-30 |
Marketing Category | unapproved drug other |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2020-04-29 |
Marketing End Date | 2020-04-30 |
Marketing Category | unapproved drug other |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2020-04-29 |
Marketing End Date | 2020-04-30 |
Marketing Category | unapproved drug other |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2020-04-29 |
Marketing End Date | 2020-04-30 |