NDC 68001-212 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 68001-212 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA075994 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2014-02-04 |
| Marketing End Date | 2017-09-30 |