NDC 42549-666 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 42549-666 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA075317 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2004-12-20 |
| Inactivation Date | 2019-11-13 |