NDC 54868-6106 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 54868-6106 |
| Marketing Category | / |
| Marketing Category | NDA |
| Application Number | NDA021620 |
| Product Type | HUMAN OTC DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2010-04-19 |
| Inactivation Date | 2019-09-24 |