NDC 0006-3845 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 0006-3845 |
| Marketing Category | / |
| Marketing Category | NDA |
| Application Number | NDA021337 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2001-11-21 |
| Marketing End Date | 2018-07-31 |
| Marketing Category | NDA |
| Application Number | NDA021337 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2010-06-04 |
| Marketing End Date | 2018-07-31 |