NDC 60258-850 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 60258-850 |
Marketing Category | / |
Marketing Category | ANDA |
Application Number | ANDA040644 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2010-06-15 |
Marketing End Date | 2013-09-11 |
Marketing Category | ANDA |
Application Number | ANDA040644 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2010-06-15 |
Marketing End Date | 2013-09-11 |