NDC 11822-8157 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 11822-8157 |
| Marketing Category | / |
| Marketing Category | NDA |
| Application Number | NDA021620 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2017-09-05 |
| Marketing End Date | 2017-09-06 |