NDC 63010-011 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 63010-011 |
| Marketing Category | / |
| Marketing Category | NDA |
| Application Number | NDA020778 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 1997-03-14 |
| Marketing End Date | 2011-11-30 |