NDC 68084-160 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 68084-160 |
Marketing Category | / |
Marketing Category | ANDA |
Application Number | ANDA074769 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2013-08-05 |
Marketing End Date | 2015-05-08 |
Marketing Category | ANDA |
Application Number | ANDA074769 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2013-08-05 |
Marketing End Date | 2015-05-08 |