NDC 54868-5262 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 54868-5262 |
Marketing Category | / |
Marketing Category | NDA |
Application Number | NDA021410 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2005-08-25 |
Marketing End Date | 2012-06-30 |
Marketing Category | NDA |
Application Number | NDA021410 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2005-08-25 |
Marketing End Date | 2012-06-30 |