NDC 67544-001 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 67544-001 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA040419 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2011-07-06 |
| Marketing End Date | 2019-02-25 |