NDC 63717-901 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 63717-901 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA076642 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2008-12-16 |
| Marketing End Date | 2014-04-20 |
| Marketing Category | ANDA |
| Application Number | ANDA076642 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2008-12-16 |
| Marketing End Date | 2014-04-20 |