NDC 54868-5651 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 54868-5651 |
Marketing Category | / |
Marketing Category | ANDA |
Application Number | ANDA077927 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2010-11-09 |
Inactivation Date | 2019-09-24 |
Marketing Category | ANDA |
Application Number | ANDA077927 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2006-08-07 |
Inactivation Date | 2019-09-24 |
Marketing Category | ANDA |
Application Number | ANDA077927 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2011-02-22 |
Inactivation Date | 2019-09-24 |
Marketing Category | ANDA |
Application Number | ANDA077927 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2006-08-07 |
Inactivation Date | 2019-09-24 |
Marketing Category | ANDA |
Application Number | ANDA077927 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2006-08-07 |
Inactivation Date | 2019-09-24 |