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 |