NDC 51079-468 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 51079-468 |
Marketing Category | / |
Marketing Category | ANDA |
Application Number | ANDA078855 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2008-05-01 |
Marketing End Date | 2018-12-31 |
Marketing Category | ANDA |
Application Number | ANDA078855 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2008-05-01 |
Marketing End Date | 2018-12-31 |