NDC 50242-073 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 50242-073 |
| Marketing Category | / |
| Marketing Category | NDA |
| Application Number | NDA020522 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | ML |
| Marketing Start Date | 1995-12-29 |
| Marketing End Date | 2016-07-31 |