NDC 16714-342 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 16714-342 |
Marketing Category | / |
Marketing Category | ANDA |
Application Number | ANDA091368 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2013-02-04 |
Marketing End Date | 2015-10-31 |
Marketing Category | ANDA |
Application Number | ANDA091368 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2013-02-04 |
Marketing End Date | 2015-10-31 |
Marketing Category | ANDA |
Application Number | ANDA091368 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2013-02-04 |
Marketing End Date | 2015-10-31 |
Marketing Category | ANDA |
Application Number | ANDA091368 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2013-02-04 |
Marketing End Date | 2015-10-31 |
Marketing Category | ANDA |
Application Number | ANDA091368 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2013-02-04 |
Marketing End Date | 2015-10-31 |