NDC 55154-5472 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 55154-5472 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA075491 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2000-07-01 |
| Marketing End Date | 2016-03-30 |