NDC 0245-0182 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 0245-0182 |
Marketing Category | / |
Marketing Category | ANDA |
Application Number | ANDA078182 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2011-01-21 |
Marketing End Date | 2016-06-30 |
Marketing Category | ANDA |
Application Number | ANDA078182 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2011-01-21 |
Marketing End Date | 2016-06-30 |
Marketing Category | ANDA |
Application Number | ANDA078182 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2011-02-07 |
Marketing End Date | 2016-06-30 |
Marketing Category | ANDA |
Application Number | ANDA078182 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2011-01-21 |
Marketing End Date | 2016-06-30 |