NDC 54868-4697 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 54868-4697 |
Marketing Category | / |
Marketing Category | ANDA |
Application Number | ANDA040075 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2013-01-10 |
Marketing End Date | 2013-02-06 |
Marketing Category | ANDA |
Application Number | ANDA040075 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | ML |
Marketing Start Date | 2013-01-10 |
Inactivation Date | 2019-09-24 |