NDC 63162-518 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 63162-518 |
| Marketing Category | / |
| Marketing Category | OTC monograph not final |
| Application Number | part343 |
| Product Type | HUMAN OTC DRUG |
| Billing Unit | ML |
| Marketing Start Date | 1997-04-01 |
| Inactivation Date | 2019-11-27 |