NDC 60429-389 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 60429-389 |
Marketing Category | / |
Marketing Category | ANDA |
Application Number | ANDA077081 |
Product Type | HUMAN OTC DRUG |
Billing Unit | EA |
Marketing Start Date | 2014-03-20 |
Marketing End Date | 2018-04-11 |
Marketing Category | ANDA |
Application Number | ANDA077081 |
Product Type | HUMAN OTC DRUG |
Billing Unit | EA |
Marketing Start Date | 2014-03-20 |
Marketing End Date | 2018-04-11 |