NDC 68682-409 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 68682-409 |
| Marketing Category | / |
| Marketing Category | NDA authorized generic |
| Application Number | NDA012750 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2009-09-28 |
| Marketing End Date | 2019-02-28 |