NDC 0338-1083 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 0338-1083 |
| Marketing Category | / |
| Marketing Category | NDA |
| Application Number | NDA020734 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 1997-09-29 |
| Marketing End Date | 2018-05-14 |