NDC 68016-282 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 68016-282 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA074507 |
| Product Type | HUMAN OTC DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2013-09-01 |
| Marketing End Date | 2018-09-30 |