NDC 42023-126 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 42023-126 |
| Marketing Category | / |
| Marketing Category | NDA |
| Application Number | NDA017443 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2008-08-01 |
| Marketing End Date | 2015-07-31 |