NDC 64376-650 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 64376-650 |
Marketing Category | / |
Marketing Category | ANDA |
Application Number | ANDA040747 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2010-09-07 |
Marketing End Date | 2018-09-30 |
Marketing Category | ANDA |
Application Number | ANDA040747 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2010-09-07 |
Marketing End Date | 2018-09-30 |
Marketing Category | ANDA |
Application Number | ANDA040747 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2010-09-07 |
Marketing End Date | 2013-09-10 |
Marketing Category | ANDA |
Application Number | ANDA040747 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2010-09-07 |
Marketing End Date | 2018-09-30 |