NDC 54868-6270 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 54868-6270 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA078104 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | GM |
| Marketing Start Date | 2011-09-14 |
| Inactivation Date | 2019-09-24 |