NDC 0169-2312 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 0169-2312 |
| Marketing Category | / |
| Marketing Category | NDA |
| Application Number | NDA021536 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2015-12-31 |
| Marketing End Date | 2009-09-29 |