NDC 17478-216 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 17478-216 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA083590 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | ML |
| Marketing Start Date | 1995-12-19 |
| Marketing End Date | 2017-09-30 |