NDC 0179-0095 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 0179-0095 |
Marketing Category | / |
Marketing Category | ANDA |
Application Number | ANDA090200 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2011-06-07 |
Marketing End Date | 2013-02-28 |
Marketing Category | ANDA |
Application Number | ANDA090200 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2011-06-07 |
Marketing End Date | 2013-02-28 |