NDC 51672-4050 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 51672-4050 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA075687 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2000-10-24 |
| Marketing End Date | 2014-10-17 |
| Marketing Category | ANDA |
| Application Number | ANDA075687 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2000-10-24 |
| Marketing End Date | 2014-10-17 |