NDC 0093-0784 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 0093-0784 |
Marketing Category | / |
Marketing Category | ANDA |
Application Number | ANDA075797 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2003-02-20 |
Marketing End Date | 2018-02-28 |
Marketing Category | ANDA |
Application Number | ANDA075797 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2008-01-09 |
Marketing End Date | 2017-09-30 |
Marketing Category | ANDA |
Application Number | ANDA075797 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2003-02-20 |
Marketing End Date | 2018-02-28 |
Marketing Category | ANDA |
Application Number | ANDA075797 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2008-01-09 |
Marketing End Date | 2018-02-28 |