NDC 50730-2113 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 50730-2113 |
Marketing Category | / |
Marketing Category | OTC monograph not final |
Application Number | part334 |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 1996-05-22 |
Marketing End Date | 2010-05-31 |