NDC 54868-5983 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 54868-5983 |
Marketing Category | / |
Marketing Category | NDA |
Application Number | NDA021990 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2010-01-06 |
Inactivation Date | 2019-09-24 |
Marketing Category | NDA |
Application Number | NDA021990 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2009-06-22 |
Inactivation Date | 2019-09-24 |