NDC 59762-1301 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 59762-1301 |
Marketing Category | / |
Marketing Category | ANDA |
Application Number | ANDA077739 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2007-09-11 |
Marketing End Date | 2016-03-31 |
Marketing Category | ANDA |
Application Number | ANDA077739 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2007-09-11 |
Marketing End Date | 2016-03-31 |