NDC 63783-3233 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 63783-3233 |
| Marketing Category | / |
| Marketing Category | OTC monograph final |
| Application Number | part355 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2011-09-01 |
| Marketing End Date | 2012-01-27 |