NDC 41167-4233 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 41167-4233 |
| Marketing Category | / |
| Marketing Category | NDA |
| Application Number | NDA021909 |
| Product Type | HUMAN OTC DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2011-03-03 |
| Marketing End Date | 2018-01-02 |