NDC 0406-1772 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 0406-1772 |
Marketing Category | / |
Marketing Category | ANDA |
Application Number | ANDA075738 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2009-06-08 |
Marketing End Date | 2009-08-20 |
Marketing Category | ANDA |
Application Number | ANDA075738 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2009-06-08 |
Marketing End Date | 2011-07-31 |
Marketing Category | ANDA |
Application Number | ANDA075738 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2009-06-08 |
Marketing End Date | 2011-07-31 |
Marketing Category | ANDA |
Application Number | ANDA075738 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2009-06-08 |
Marketing End Date | 2011-07-31 |
Marketing Category | ANDA |
Application Number | ANDA075738 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2009-06-08 |
Marketing End Date | 2011-07-31 |
Marketing Category | ANDA |
Application Number | ANDA075738 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2009-06-08 |
Marketing End Date | 2009-08-20 |