NDC 16714-232 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 16714-232 |
Marketing Category | / |
Marketing Category | ANDA |
Application Number | ANDA065359 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2009-06-02 |
Marketing End Date | 2014-03-31 |
Marketing Category | ANDA |
Application Number | ANDA065359 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2009-06-02 |
Marketing End Date | 2014-03-31 |