NDC 42192-520 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 42192-520 |
Marketing Category | / |
Marketing Category | unapproved drug other |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | ML |
Marketing Start Date | 2011-05-06 |
Marketing End Date | 2013-10-31 |