NDC 47682-702 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 47682-702 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA079174 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2014-11-17 |
| Marketing End Date | 2017-04-03 |
| Marketing Category | ANDA |
| Application Number | ANDA079174 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2017-02-01 |
| Marketing End Date | 2017-04-03 |