NDC 0409-7122 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 0409-7122 |
| Marketing Category | / |
| Marketing Category | NDA |
| Application Number | NDA020041 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | ML |
| Marketing Start Date | 1991-12-19 |
| Marketing End Date | 2011-10-01 |