NDC 0591-3760 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 0591-3760 |
Marketing Category | / |
Marketing Category | ANDA |
Application Number | ANDA077890 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2010-10-15 |
Marketing End Date | 2018-12-31 |
Marketing Category | ANDA |
Application Number | ANDA077890 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2010-10-15 |
Marketing End Date | 2018-12-31 |