NDC 0781-5526 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 0781-5526 |
Marketing Category | / |
Marketing Category | ANDA |
Application Number | ANDA090288 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2010-07-07 |
Marketing End Date | 2010-07-07 |