NDC 0093-4029 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 0093-4029 |
Marketing Category | / |
Marketing Category | ANDA |
Application Number | ANDA070719 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2007-12-14 |
Marketing End Date | 2017-01-31 |
Marketing Category | ANDA |
Application Number | ANDA070719 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2007-12-14 |
Marketing End Date | 2013-10-25 |
Marketing Category | ANDA |
Application Number | ANDA070719 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2007-12-14 |
Marketing End Date | 2017-01-31 |
Marketing Category | ANDA |
Application Number | ANDA070719 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2007-12-14 |
Marketing End Date | 2013-10-25 |