NDC 63304-657 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 63304-657 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA065007 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 1998-07-28 |
| Marketing End Date | 2011-08-29 |
| Marketing Category | ANDA |
| Application Number | ANDA065007 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 1998-07-28 |
| Marketing End Date | 2011-08-29 |
| Marketing Category | ANDA |
| Application Number | ANDA065007 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 1998-07-28 |
| Marketing End Date | 2011-08-29 |