NDC 63304-972 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 63304-972 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA065115 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2005-08-30 |
| Inactivation Date | 2019-11-27 |