NDC 0186-0110 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 0186-0110 |
| Marketing Category | / |
| Marketing Category | NDA |
| Application Number | NDA010418 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 1990-09-30 |
| Marketing End Date | 2014-05-31 |