NDC 69336-831 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 69336-831 |
| Marketing Category | / |
| Marketing Category | premarket notification |
| Application Number | K020540 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2018-01-02 |
| Marketing End Date | 2018-01-17 |
| Marketing Category | premarket notification |
| Application Number | K020540 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | GM |
| Marketing Start Date | 2018-01-02 |
| Inactivation Date | 2020-01-31 |