NDC 49884-196 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 49884-196 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA078671 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2010-09-14 |
| Marketing End Date | 2013-11-30 |
| Marketing Category | ANDA |
| Application Number | ANDA078671 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2010-09-14 |
| Marketing End Date | 2014-09-30 |