NDC 0074-3315 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 0074-3315 |
| Marketing Category | / |
| Marketing Category | NDA |
| Application Number | NDA022078 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2008-02-15 |
| Marketing End Date | 2017-10-31 |