NDC 0338-1109 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 0338-1109 |
| Marketing Category | / |
| Marketing Category | NDA |
| Application Number | NDA020678 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | ML |
| Marketing Start Date | 1997-03-26 |
| Marketing End Date | 2018-05-14 |