NDC 68084-520 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 68084-520 |
Marketing Category | / |
Marketing Category | ANDA |
Application Number | ANDA086242 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2011-09-19 |
Marketing End Date | 2018-07-31 |
Marketing Category | ANDA |
Application Number | ANDA086242 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2015-12-28 |
Marketing End Date | 2018-07-31 |
Marketing Category | ANDA |
Application Number | ANDA086242 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2016-01-01 |
Marketing End Date | 2018-07-31 |
Marketing Category | ANDA |
Application Number | ANDA086242 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2011-09-19 |
Marketing End Date | 2016-02-29 |