NDC 68453-900 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 68453-900 |
| Marketing Category | / |
| Marketing Category | NDA |
| Application Number | NDA020353 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2009-10-15 |
| Marketing End Date | 2013-10-31 |