NDC 50090-2110 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 50090-2110 |
Marketing Category | / |
Marketing Category | ANDA |
Application Number | ANDA078888 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2015-10-14 |
Marketing End Date | 2018-06-30 |
Marketing Category | ANDA |
Application Number | ANDA078888 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2015-10-14 |
Marketing End Date | 2018-05-31 |
Marketing Category | ANDA |
Application Number | ANDA078888 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2015-10-14 |
Marketing End Date | 2018-06-30 |
Marketing Category | ANDA |
Application Number | ANDA078888 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2015-10-14 |
Marketing End Date | 2018-05-31 |
Marketing Category | ANDA |
Application Number | ANDA078888 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2015-10-14 |
Marketing End Date | 2018-06-30 |