NDC 63739-283 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 63739-283 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA074984 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2010-05-24 |
| Marketing End Date | 2017-01-05 |
| Marketing Category | ANDA |
| Application Number | ANDA074984 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2007-07-24 |
| Marketing End Date | 2017-01-05 |