NDC 67457-478 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 67457-478 |
Marketing Category | / |
Marketing Category | ANDA |
Application Number | ANDA200170 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2014-05-22 |
Marketing End Date | 2018-08-31 |