NDC 55154-7135 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 55154-7135 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA078558 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2013-10-14 |
| Marketing End Date | 2017-12-31 |