NDC 63323-175 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 63323-175 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA078810 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2009-09-17 |
| Marketing End Date | 2010-07-16 |