NDC 16590-064 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 16590-064 |
Marketing Category | / |
Marketing Category | NDA |
Application Number | NDA020685 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 1996-03-13 |
Inactivation Date | 2019-11-13 |