NDC 63717-902 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 63717-902 |
Marketing Category | / |
Marketing Category | ANDA |
Application Number | ANDA076642 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2008-12-16 |
Marketing End Date | 2014-10-17 |
Marketing Category | ANDA |
Application Number | ANDA076642 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2008-12-16 |
Marketing End Date | 2014-10-17 |