NDC 73391-0003 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 73391-0003 |
| Marketing Category | / |
| Marketing Category | OTC monograph final |
| Application Number | part352 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2019-11-01 |
| Marketing End Date | 2019-11-06 |