NDC 50419-703 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 50419-703 |
| Marketing Category | / |
| Marketing Category | NDA |
| Application Number | NDA020198 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 1993-04-21 |
| Marketing End Date | 2017-11-10 |