NDC 0781-2233 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 0781-2233 |
Marketing Category | / |
Marketing Category | ANDA |
Application Number | ANDA075757 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2003-01-28 |
Marketing End Date | 2017-02-28 |
Marketing Category | ANDA |
Application Number | ANDA075757 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2003-01-28 |
Marketing End Date | 2017-02-28 |
Marketing Category | ANDA |
Application Number | ANDA075757 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2003-01-28 |
Marketing End Date | 2017-02-28 |
Marketing Category | ANDA |
Application Number | ANDA075757 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2003-01-28 |
Marketing End Date | 2017-02-28 |