NDC 63323-317 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 63323-317 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA078522 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | ML |
| Marketing Start Date | 2009-11-20 |
| Marketing End Date | 2016-05-31 |