NDC 60429-120 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 60429-120 |
Marketing Category | / |
Marketing Category | ANDA |
Application Number | ANDA076729 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | ML |
Marketing Start Date | 2011-07-20 |
Marketing End Date | 2014-05-15 |