NDC 0008-0606 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 0008-0606 |
Marketing Category | / |
Marketing Category | NDA |
Application Number | NDA020987 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2008-01-31 |
Marketing End Date | 2017-09-30 |