NDC 61314-395 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 61314-395 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA084109 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2002-08-22 |
| Marketing End Date | 2016-09-02 |