NDC 42549-542 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 42549-542 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA074131 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2011-10-07 |
| Inactivation Date | 2019-11-13 |