NDC 69650-002 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 69650-002 |
Marketing Category | / |
Marketing Category | unapproved drug other |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2015-03-31 |
Marketing Category | unapproved drug other |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2015-03-31 |
Inactivation Date | 2020-01-31 |