NDC 68382-228 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 68382-228 |
| Marketing Category | / |
| Marketing Category | NDA authorized generic |
| Application Number | NDA021656 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2004-11-05 |
| Marketing End Date | 2018-11-03 |