NDC 60258-860 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 60258-860 |
Marketing Category | / |
Marketing Category | ANDA |
Application Number | ANDA078488 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | ML |
Marketing Start Date | 2008-10-06 |
Marketing End Date | 2013-09-11 |
Marketing Category | ANDA |
Application Number | ANDA078488 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | ML |
Marketing Start Date | 2008-10-06 |
Marketing End Date | 2013-09-11 |