NDC 42023-145 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 42023-145 |
| Marketing Category | / |
| Marketing Category | NDA AUTHORIZED GENERIC |
| Application Number | NDA017443 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2013-04-08 |
| Marketing End Date | 2017-10-31 |