NDC 68084-900 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 68084-900 |
Marketing Category | / |
Marketing Category | ANDA |
Application Number | ANDA077653 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2015-02-15 |
Marketing End Date | 2016-04-26 |
Marketing Category | ANDA |
Application Number | ANDA077653 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2015-02-15 |
Marketing End Date | 2018-11-30 |
Marketing Category | ANDA |
Application Number | ANDA077653 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2015-09-01 |
Marketing End Date | 2018-11-30 |
Marketing Category | ANDA |
Application Number | ANDA077653 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2015-09-01 |
Marketing End Date | 2018-11-30 |