NDC 55111-609 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 55111-609 |
Marketing Category | / |
Marketing Category | ANDA |
Application Number | ANDA090723 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2014-06-18 |
Marketing End Date | 2016-06-17 |
Marketing Category | ANDA |
Application Number | ANDA090723 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2014-06-18 |
Marketing End Date | 2016-06-17 |
Marketing Category | ANDA |
Application Number | ANDA090723 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2014-06-18 |
Marketing End Date | 2016-06-17 |
Marketing Category | ANDA |
Application Number | ANDA090723 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2014-06-18 |
Marketing End Date | 2016-06-17 |
Marketing Category | ANDA |
Application Number | ANDA090723 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2014-06-18 |
Marketing End Date | 2016-06-17 |