NDC 63323-345 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 63323-345 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA065329 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2011-06-20 |
| Marketing End Date | 2017-12-01 |