NDC 68405-118 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 68405-118 |
Marketing Category | / |
Marketing Category | unapproved drug other |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2011-03-03 |
Inactivation Date | 2019-10-29 |