NDC 0066-9850 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 0066-9850 |
| Marketing Category | / |
| Marketing Category | NDA |
| Application Number | NDA020743 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | GM |
| Marketing Start Date | 1997-09-26 |
| Marketing End Date | 2014-12-31 |