NDC 50090-1015 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 50090-1015 |
Marketing Category | / |
Marketing Category | ANDA |
Application Number | ANDA077851 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2014-11-28 |
Marketing End Date | 2019-03-31 |
Marketing Category | ANDA |
Application Number | ANDA077851 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2014-11-28 |
Marketing End Date | 2019-03-31 |
Marketing Category | ANDA |
Application Number | ANDA077851 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2014-11-28 |
Marketing End Date | 2019-03-31 |
Marketing Category | ANDA |
Application Number | ANDA077851 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2014-11-28 |
Marketing End Date | 2019-03-31 |
Marketing Category | ANDA |
Application Number | ANDA077851 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2014-11-28 |
Marketing End Date | 2019-03-31 |