NDC 0074-4317 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 0074-4317 |
| Marketing Category | / |
| Marketing Category | NDA |
| Application Number | NDA021606 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2010-06-14 |
| Marketing End Date | 2014-09-03 |
| Marketing Category | NDA |
| Application Number | NDA021606 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2010-06-14 |
| Marketing End Date | 2014-05-22 |
| Marketing Category | NDA |
| Application Number | NDA021606 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2009-10-30 |
| Marketing End Date | 2014-09-03 |