NDC 52183-383 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 52183-383 |
| Marketing Category | / |
| Marketing Category | OTC MONOGRAPH NOT FINAL |
| Application Number | part343 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2010-07-28 |
| Inactivation Date | 2019-10-29 |