NDC 55154-5112 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 55154-5112 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA083312 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 1973-09-19 |
| Marketing End Date | 2017-10-31 |