NDC 0603-3740 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 0603-3740 |
Marketing Category | / |
Marketing Category | ANDA |
Application Number | ANDA076796 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2004-03-26 |
Marketing End Date | 2016-04-21 |
Marketing Category | ANDA |
Application Number | ANDA076796 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2004-03-26 |
Marketing End Date | 2018-09-30 |
Marketing Category | ANDA |
Application Number | ANDA076796 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2004-03-26 |
Marketing End Date | 2018-09-30 |
Marketing Category | ANDA |
Application Number | ANDA076796 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2004-03-26 |
Marketing End Date | 2018-09-30 |