NDC 68084-052 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 68084-052 |
Marketing Category | / |
Marketing Category | ANDA |
Application Number | ANDA074984 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2013-03-26 |
Marketing End Date | 2017-12-31 |
Marketing Category | ANDA |
Application Number | ANDA074984 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2013-04-15 |
Marketing End Date | 2018-09-30 |
Marketing Category | ANDA |
Application Number | ANDA074984 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2013-04-17 |
Marketing End Date | 2018-09-30 |
Marketing Category | ANDA |
Application Number | ANDA074984 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2013-03-26 |
Marketing End Date | 2017-12-31 |