NDC 55154-9359 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 55154-9359 |
Marketing Category | / |
Marketing Category | NDA |
Application Number | NDA017029 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2010-06-18 |
Marketing End Date | 2013-06-30 |