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 |