NDC 54868-4730 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 54868-4730 |
Marketing Category | / |
Marketing Category | NDA |
Application Number | NDA021241 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2003-01-23 |
Inactivation Date | 2019-09-24 |