NDC 68084-053 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 68084-053 |
Marketing Category | / |
Marketing Category | ANDA |
Application Number | ANDA074984 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2013-04-19 |
Marketing End Date | 2018-09-30 |
Marketing Category | ANDA |
Application Number | ANDA074984 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2013-03-14 |
Marketing End Date | 2018-08-31 |
Marketing Category | ANDA |
Application Number | ANDA074984 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2013-03-10 |
Marketing End Date | 2018-08-31 |
Marketing Category | ANDA |
Application Number | ANDA074984 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2013-04-19 |
Marketing End Date | 2018-09-30 |