NDC 54868-5870 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 54868-5870 |
| Marketing Category | / |
| Marketing Category | OTC monograph final |
| Application Number | part347 |
| Product Type | HUMAN OTC DRUG |
| Billing Unit | GM |
| Marketing Start Date | 2008-03-28 |
| Inactivation Date | 2019-09-24 |