NDC 0078-0442 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 0078-0442 |
| Marketing Category | / |
| Marketing Category | NDA |
| Application Number | NDA018029 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 1982-03-31 |
| Marketing End Date | 2015-02-28 |