NDC 63629-2871 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 63629-2871 |
Marketing Category | / |
Marketing Category | ANDA |
Application Number | ANDA065228 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2005-07-13 |
Marketing End Date | 2011-11-01 |