NDC 37808-923 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 37808-923 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA077958 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2010-09-10 |
| Marketing End Date | 2015-06-01 |