NDC 16590-032 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 16590-032 |
Marketing Category | / |
Marketing Category | ANDA |
Application Number | ANDA019137 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | GM |
Marketing Start Date | 1984-02-26 |
Inactivation Date | 2020-01-31 |