NDC 42808-101 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 42808-101 |
Marketing Category | / |
Marketing Category | unapproved drug other |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2011-08-01 |
Marketing End Date | 2017-08-22 |