NDC 0517-0805 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 0517-0805 |
Marketing Category | / |
Marketing Category | UNAPPROVED DRUG OTHER |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | ML |
Marketing Start Date | 1992-11-01 |
Marketing End Date | 2012-03-01 |