NDC 0186-1031 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 0186-1031 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA070552 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 1990-07-01 |
| Marketing End Date | 2014-04-30 |