NDC 49884-600 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 49884-600 |
Marketing Category | / |
Marketing Category | NDA |
Application Number | NDA018578 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 1997-06-27 |
Marketing End Date | 2014-01-31 |
Marketing Category | NDA |
Application Number | NDA018578 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 1997-09-22 |
Marketing End Date | 2014-02-28 |
Marketing Category | NDA |
Application Number | NDA018578 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 1997-06-27 |
Marketing End Date | 2014-01-31 |
Marketing Category | NDA |
Application Number | NDA018578 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 1997-06-27 |
Marketing End Date | 2013-09-25 |
Marketing Category | NDA |
Application Number | NDA018578 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 1997-09-29 |
Marketing End Date | 2014-03-31 |