NDC 16714-583 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 16714-583 |
Marketing Category | / |
Marketing Category | ANDA |
Application Number | ANDA090382 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2010-10-03 |
Marketing End Date | 2015-03-31 |
Marketing Category | ANDA |
Application Number | ANDA090382 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2010-10-03 |
Marketing End Date | 2015-03-31 |
Marketing Category | ANDA |
Application Number | ANDA090382 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2010-10-03 |
Marketing End Date | 2015-03-31 |