NDC 50268-382 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 50268-382 |
| Marketing Category | / |
| Marketing Category | OTC monograph final |
| Application Number | part341 |
| Product Type | HUMAN OTC DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2016-10-04 |
| Marketing End Date | 2019-01-02 |
| Marketing Category | OTC monograph final |
| Application Number | part341 |
| Product Type | HUMAN OTC DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2016-10-04 |
| Marketing End Date | 2019-01-02 |