NDC 53329-820 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 53329-820 |
| Marketing Category | / |
| Marketing Category | OTC monograph not final |
| Application Number | part333A |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2009-09-15 |
| Marketing End Date | 2017-12-31 |
| Marketing Category | OTC monograph not final |
| Application Number | part333A |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2007-01-01 |
| Marketing End Date | 2012-12-17 |
| Marketing Category | OTC monograph not final |
| Application Number | part333A |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2012-12-17 |
| Marketing End Date | 2017-12-31 |
| Marketing Category | OTC monograph not final |
| Application Number | part333A |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2007-01-01 |
| Marketing End Date | 2012-12-17 |