NDC 51079-806 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 51079-806 |
Marketing Category | / |
Marketing Category | ANDA |
Application Number | ANDA091176 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2010-08-13 |
Marketing End Date | 2018-11-30 |
Marketing Category | ANDA |
Application Number | ANDA091176 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2010-08-13 |
Marketing End Date | 2018-11-30 |