NDC 50742-108 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 50742-108 |
Marketing Category | / |
Marketing Category | ANDA |
Application Number | ANDA078459 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2011-05-01 |
Marketing End Date | 2016-05-31 |
Marketing Category | ANDA |
Application Number | ANDA078459 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2011-05-01 |
Marketing End Date | 2016-05-31 |