NDC 58118-0159 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 58118-0159 |
Marketing Category | / |
Marketing Category | ANDA |
Application Number | ANDA075576 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2009-01-21 |
Marketing End Date | 2017-02-22 |
Marketing Category | ANDA |
Application Number | ANDA075576 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2009-01-21 |
Marketing End Date | 2017-02-22 |
Marketing Category | ANDA |
Application Number | ANDA075576 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2009-01-21 |
Marketing End Date | 2017-02-22 |
Marketing Category | ANDA |
Application Number | ANDA075576 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2009-01-21 |
Marketing End Date | 2017-02-22 |