NDC 0186-5022 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 0186-5022 |
| Marketing Category | / |
| Marketing Category | NDA |
| Application Number | NDA021153 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2001-03-19 |
| Marketing End Date | 2015-07-16 |