NDC 0093-4742 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 0093-4742 |
Marketing Category | / |
Marketing Category | ANDA |
Application Number | ANDA077048 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2008-02-13 |
Marketing End Date | 2016-03-31 |
Marketing Category | ANDA |
Application Number | ANDA077048 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2007-11-08 |
Marketing End Date | 2015-10-31 |
Marketing Category | ANDA |
Application Number | ANDA077048 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2007-11-08 |
Marketing End Date | 2016-03-31 |
Marketing Category | ANDA |
Application Number | ANDA077048 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2008-03-21 |
Marketing End Date | 2013-08-31 |
Marketing Category | ANDA |
Application Number | ANDA077048 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2008-01-17 |
Marketing End Date | 2016-03-31 |