NDC 63323-734 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 63323-734 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA076207 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | ML |
| Marketing Start Date | 2002-05-19 |
| Marketing End Date | 2015-08-27 |