NDC 58232-0723 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 58232-0723 |
| Marketing Category | / |
| Marketing Category | OTC MONOGRAPH FINAL |
| Application Number | part347 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2013-07-15 |
| Marketing End Date | 2018-05-01 |
| Marketing Category | OTC MONOGRAPH FINAL |
| Application Number | part347 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2013-07-15 |
| Marketing End Date | 2018-05-01 |
| Marketing Category | OTC MONOGRAPH FINAL |
| Application Number | part347 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2013-07-15 |
| Marketing End Date | 2018-05-01 |
| Marketing Category | OTC MONOGRAPH FINAL |
| Application Number | part347 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2013-07-15 |
| Marketing End Date | 2018-05-01 |
| Marketing Category | OTC MONOGRAPH FINAL |
| Application Number | part347 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2013-07-15 |
| Marketing End Date | 2018-05-01 |
| Marketing Category | OTC MONOGRAPH FINAL |
| Application Number | part347 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2013-07-15 |
| Marketing End Date | 2018-05-01 |
| Marketing Category | OTC MONOGRAPH FINAL |
| Application Number | part347 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2013-07-15 |
| Marketing End Date | 2018-05-01 |