NDC 51079-854 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 51079-854 |
Marketing Category | / |
Marketing Category | ANDA |
Application Number | ANDA077590 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2009-11-09 |
Marketing End Date | 2016-11-30 |
Marketing Category | ANDA |
Application Number | ANDA077590 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2009-11-09 |
Marketing End Date | 2016-11-30 |