NDC 0603-3968 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 0603-3968 |
Marketing Category | / |
Marketing Category | ANDA |
Application Number | ANDA040574 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2005-05-27 |
Marketing End Date | 2017-03-31 |
Marketing Category | ANDA |
Application Number | ANDA040574 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2005-05-27 |
Marketing End Date | 2016-01-28 |
Marketing Category | ANDA |
Application Number | ANDA040574 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2005-05-27 |
Marketing End Date | 2017-03-31 |
Marketing Category | ANDA |
Application Number | ANDA040574 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2005-05-27 |
Marketing End Date | 2017-03-31 |