NDC 60429-720 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 60429-720 |
Marketing Category | / |
Marketing Category | ANDA |
Application Number | ANDA075805 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2010-12-20 |
Marketing End Date | 2016-12-30 |
Marketing Category | ANDA |
Application Number | ANDA075805 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2011-12-20 |
Marketing End Date | 2016-12-30 |