NDC 54868-5736 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 54868-5736 |
Marketing Category | / |
Marketing Category | ANDA |
Application Number | ANDA077715 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2009-11-09 |
Inactivation Date | 2019-09-24 |
Marketing Category | ANDA |
Application Number | ANDA077715 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2009-07-23 |
Inactivation Date | 2019-09-24 |