NDC 69189-4246 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 69189-4246 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA077754 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2015-05-01 |
| Inactivation Date | 2020-01-31 |
| Marketing Category | ANDA |
| Application Number | ANDA077754 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2015-05-01 |
| Inactivation Date | 2020-01-31 |