NDC 50090-1235 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 50090-1235 |
| Marketing Category | / |
| Marketing Category | NDA |
| Application Number | NDA020872 |
| Product Type | HUMAN OTC DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2014-11-28 |
| Marketing End Date | 2019-02-28 |