NDC 67732-403 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 67732-403 |
Marketing Category | / |
Marketing Category | OTC monograph not final |
Application Number | part352 |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2012-11-13 |
Inactivation Date | 2020-01-31 |