NDC 68084-388 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 68084-388 |
Marketing Category | / |
Marketing Category | ANDA |
Application Number | ANDA040715 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2009-12-18 |
Marketing End Date | 2018-10-31 |
Marketing Category | ANDA |
Application Number | ANDA040715 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2009-12-18 |
Marketing End Date | 2018-10-31 |