NDC 50268-103 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 50268-103 |
Marketing Category | / |
Marketing Category | ANDA |
Application Number | ANDA065507 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2016-11-16 |
Marketing End Date | 2018-12-31 |
Marketing Category | ANDA |
Application Number | ANDA065507 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2016-11-16 |
Marketing End Date | 2018-12-31 |