NDC 55154-5588 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 55154-5588 |
Marketing Category | / |
Marketing Category | ANDA |
Application Number | ANDA074226 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2010-11-04 |
Marketing End Date | 2018-08-31 |