NDC 66479-512 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 66479-512 |
Marketing Category | / |
Marketing Category | NDA |
Application Number | NDA016862 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2009-09-25 |
Marketing End Date | 2010-11-19 |
Marketing Category | NDA |
Application Number | NDA016862 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2009-09-25 |
Marketing End Date | 2010-11-19 |