NDC 66993-106 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 66993-106 |
| Marketing Category | / |
| Marketing Category | NDA authorized generic |
| Application Number | NDA020872 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2005-09-01 |
| Marketing End Date | 2013-01-31 |