NDC 68788-6449 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 68788-6449 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA077917 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2016-08-05 |
| Marketing End Date | 2019-02-20 |
| Marketing Category | ANDA |
| Application Number | ANDA077917 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2016-08-05 |
| Marketing End Date | 2019-02-20 |
| Marketing Category | ANDA |
| Application Number | ANDA077917 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2016-08-05 |
| Marketing End Date | 2019-02-20 |