NDC 0555-0614 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 0555-0614 |
Marketing Category | / |
Marketing Category | ANDA |
Application Number | ANDA077724 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2010-01-04 |
Marketing End Date | 2013-11-22 |