NDC 0603-6469 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 0603-6469 |
Marketing Category | / |
Marketing Category | ANDA |
Application Number | ANDA078616 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2008-11-21 |
Marketing End Date | 2014-07-24 |
Marketing Category | ANDA |
Application Number | ANDA078616 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2008-11-21 |
Marketing End Date | 2016-12-31 |
Marketing Category | ANDA |
Application Number | ANDA078616 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2008-11-21 |
Marketing End Date | 2016-12-31 |
Marketing Category | ANDA |
Application Number | ANDA078616 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2008-11-21 |
Marketing End Date | 2016-12-31 |
Marketing Category | ANDA |
Application Number | ANDA078616 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2008-11-21 |
Marketing End Date | 2016-12-31 |
Marketing Category | ANDA |
Application Number | ANDA078616 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2008-11-21 |
Marketing End Date | 2016-12-31 |
Marketing Category | ANDA |
Application Number | ANDA078616 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2008-11-21 |
Marketing End Date | 2016-12-31 |
Marketing Category | ANDA |
Application Number | ANDA078616 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2008-11-21 |
Marketing End Date | 2014-07-24 |
Marketing Category | ANDA |
Application Number | ANDA078616 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2008-11-21 |
Marketing End Date | 2016-12-31 |