NDC 55292-102 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 55292-102 |
| Marketing Category | / |
| Marketing Category | NDA |
| Application Number | NDA005378 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 1943-12-31 |
| Marketing End Date | 2017-08-19 |