NDC 0338-1071 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 0338-1071 |
| Marketing Category | / |
| Marketing Category | NDA |
| Application Number | NDA020255 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 1993-09-27 |
| Marketing End Date | 2008-12-31 |