NDC 55292-302 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 55292-302 |
| Marketing Category | / |
| Marketing Category | NDA |
| Application Number | NDA017105 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 1972-06-23 |
| Marketing End Date | 2018-04-19 |