NDC 49884-108 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 49884-108 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA079234 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2003-05-28 |
| Marketing End Date | 2011-08-10 |
| Marketing Category | ANDA |
| Application Number | ANDA079234 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2003-05-28 |
| Marketing End Date | 2011-08-10 |