NDC 66993-077 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 66993-077 |
| Marketing Category | / |
| Marketing Category | NDA authorized generic |
| Application Number | NDA021427 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2014-01-24 |
| Marketing End Date | 2015-11-30 |