NDC 68084-526 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 68084-526 |
Marketing Category | / |
Marketing Category | ANDA |
Application Number | ANDA076255 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2012-04-25 |
Marketing End Date | 2015-09-30 |
Marketing Category | ANDA |
Application Number | ANDA076255 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2012-04-25 |
Marketing End Date | 2015-09-30 |