NDC 0093-5712 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 0093-5712 |
Marketing Category | / |
Marketing Category | ANDA |
Application Number | ANDA076345 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2007-06-14 |
Marketing End Date | 2017-05-31 |
Marketing Category | ANDA |
Application Number | ANDA076345 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2007-06-14 |
Marketing End Date | 2017-05-31 |
Marketing Category | ANDA |
Application Number | ANDA076345 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2008-05-02 |
Marketing End Date | 2013-09-30 |
Marketing Category | ANDA |
Application Number | ANDA076345 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2007-06-20 |
Marketing End Date | 2017-03-31 |