NDC 66993-935 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 66993-935 |
| Marketing Category | / |
| Marketing Category | NDA AUTHORIZED GENERIC |
| Application Number | NDA020208 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | GM |
| Marketing Start Date | 2007-03-31 |
| Marketing End Date | 2017-09-30 |