NDC 54868-3852 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 54868-3852 |
Marketing Category | / |
Marketing Category | NDA |
Application Number | NDA020132 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 1996-09-13 |
Marketing End Date | 2011-06-30 |