NDC 59762-5031 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 59762-5031 |
| Marketing Category | / |
| Marketing Category | NDA AUTHORIZED GENERIC |
| Application Number | NDA020329 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2004-06-11 |
| Marketing End Date | 2014-06-30 |