NDC 0409-5622 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 0409-5622 |
| Marketing Category | / |
| Marketing Category | NDA |
| Application Number | NDA018053 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | ML |
| Marketing Start Date | 1978-04-17 |
| Marketing End Date | 2016-08-05 |