NDC 54868-5042 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 54868-5042 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA076075 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | GM |
| Marketing Start Date | 2004-05-19 |
| Inactivation Date | 2019-09-24 |