NDC 42865-103 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 42865-103 |
Marketing Category | / |
Marketing Category | NDA |
Application Number | NDA022210 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2009-09-22 |
Marketing End Date | 2017-03-31 |
Marketing Category | NDA |
Application Number | NDA022210 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2009-09-22 |
Marketing End Date | 2017-03-31 |
Marketing Category | NDA |
Application Number | NDA022210 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2009-09-22 |
Marketing End Date | 2013-05-01 |
Marketing Category | NDA |
Application Number | NDA022210 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2009-09-22 |
Marketing End Date | 2017-03-31 |