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 |