NDC 68084-889 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 68084-889 |
Marketing Category | / |
Marketing Category | ANDA |
Application Number | ANDA078179 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2016-04-13 |
Marketing End Date | 2018-06-30 |
Marketing Category | ANDA |
Application Number | ANDA078179 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2016-04-13 |
Marketing End Date | 2018-06-30 |