NDC 0409-7808 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 0409-7808 |
| Marketing Category | / |
| Marketing Category | NDA |
| Application Number | NDA018826 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | ML |
| Marketing Start Date | 2005-06-21 |
| Marketing End Date | 2017-10-01 |
| Marketing Category | NDA |
| Application Number | NDA018826 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2018-09-27 |
| Marketing End Date | 2018-02-01 |
| Marketing Category | NDA |
| Application Number | NDA018826 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2018-09-27 |
| Marketing End Date | 2018-02-01 |
| Marketing Category | NDA |
| Application Number | NDA018826 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | ML |
| Marketing Start Date | 2005-08-08 |
| Marketing End Date | 2018-02-01 |