NDC 63739-113 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 63739-113 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA018569 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2004-10-01 |
| Marketing End Date | 2012-10-31 |