NDC 0037-5010 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 0037-5010 |
| Marketing Category | / |
| Marketing Category | NDA |
| Application Number | NDA020136 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2009-02-20 |
| Marketing End Date | 2016-01-15 |