NDC 46672-174 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 46672-174 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA089452 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2000-06-27 |
| Marketing End Date | 2018-03-02 |