NDC 0093-5379 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 0093-5379 |
Marketing Category | / |
Marketing Category | ANDA |
Application Number | ANDA090360 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2010-05-25 |
Marketing End Date | 2012-07-20 |
Marketing Category | ANDA |
Application Number | ANDA090360 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2010-05-25 |
Marketing End Date | 2014-11-30 |