NDC 63783-3233 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 63783-3233 |
Marketing Category | / |
Marketing Category | OTC monograph final |
Application Number | part355 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2011-09-01 |
Marketing End Date | 2012-01-27 |