NDC 54868-2130 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 54868-2130 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA040419 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 1994-11-22 |
| Marketing End Date | 2012-06-30 |