NDC 68084-320 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 68084-320 |
Marketing Category | / |
Marketing Category | ANDA |
Application Number | ANDA077633 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2009-07-05 |
Marketing End Date | 2017-12-31 |
Marketing Category | ANDA |
Application Number | ANDA077633 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2009-07-05 |
Marketing End Date | 2017-12-31 |