NDC 57664-136 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 57664-136 |
Marketing Category | / |
Marketing Category | ANDA |
Application Number | ANDA040865 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2009-12-29 |
Marketing End Date | 2018-03-02 |
Marketing Category | ANDA |
Application Number | ANDA040865 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2009-12-29 |
Marketing End Date | 2018-03-02 |
Marketing Category | ANDA |
Application Number | ANDA040865 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2009-12-29 |
Marketing End Date | 2018-03-02 |