NDC 63402-515 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 63402-515 |
| Marketing Category | / |
| Marketing Category | NDA |
| Application Number | NDA020837 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2004-08-01 |
| Marketing End Date | 2017-03-31 |
| Marketing Category | NDA |
| Application Number | NDA020837 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2010-06-16 |
| Marketing End Date | 2017-03-31 |