NDC 63481-621 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 63481-621 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA040341 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 1999-07-30 |
| Marketing End Date | 2013-12-31 |