NDC 0002-3237 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 0002-3237 |
Marketing Category | / |
Marketing Category | NDA |
Application Number | NDA021427 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2004-08-24 |
Marketing End Date | 2010-01-22 |
Marketing Category | NDA |
Application Number | NDA021427 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2004-08-24 |
Marketing End Date | 2010-01-22 |
Marketing Category | NDA |
Application Number | NDA021427 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2004-08-24 |
Marketing End Date | 2012-09-13 |
Marketing Category | NDA |
Application Number | NDA021427 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2004-08-24 |
Marketing End Date | 2012-09-30 |
Marketing Category | NDA |
Application Number | NDA021427 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2004-08-24 |
Marketing End Date | 2012-09-13 |
Marketing Category | NDA |
Application Number | NDA021427 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2004-08-24 |
Marketing End Date | 2012-09-13 |
Marketing Category | NDA |
Application Number | NDA021427 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2009-06-26 |
Marketing End Date | 2012-09-30 |