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 |