NDC 54868-5430 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 54868-5430 |
Marketing Category | / |
Marketing Category | ANDA |
Application Number | ANDA065136 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2005-10-05 |
Inactivation Date | 2019-09-24 |
Marketing Category | ANDA |
Application Number | ANDA065136 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2012-02-01 |
Inactivation Date | 2019-09-24 |
Marketing Category | ANDA |
Application Number | ANDA065136 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2005-10-05 |
Inactivation Date | 2019-09-24 |
Marketing Category | ANDA |
Application Number | ANDA065136 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2011-01-06 |
Inactivation Date | 2019-09-24 |
Marketing Category | ANDA |
Application Number | ANDA065136 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2005-10-05 |
Inactivation Date | 2019-09-24 |