NDC 60760-065 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 60760-065 |
Marketing Category | / |
Marketing Category | ANDA |
Application Number | ANDA077912 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2013-05-16 |
Marketing End Date | 2018-03-31 |
Marketing Category | ANDA |
Application Number | ANDA077912 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2013-05-16 |
Marketing End Date | 2018-03-31 |