NDC 55154-5412 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 55154-5412 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA071206 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 1986-11-17 |
| Marketing End Date | 2014-05-31 |