NDC 0074-3010 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 0074-3010 |
| Marketing Category | / |
| Marketing Category | NDA |
| Application Number | NDA021249 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2001-12-17 |
| Marketing End Date | 2018-01-31 |