NDC 21749-752 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 21749-752 |
Marketing Category | / |
Marketing Category | export only |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2012-08-15 |
Marketing Category | export only |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2016-01-30 |
Marketing Category | export only |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2012-08-15 |
Marketing Category | export only |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2012-08-15 |
Marketing Category | export only |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2012-01-30 |
Marketing Category | export only |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2012-01-30 |
Marketing Category | export only |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2012-08-15 |
Marketing Category | export only |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2012-08-15 |
Marketing Category | export only |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2012-08-15 |