NDC 68788-382 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 68788-382 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA071012 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 1987-02-03 |
| Marketing End Date | 2011-02-15 |