NDC 59762-5032 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 59762-5032 |
| 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 | 2017-01-31 |
| 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 | 2016-08-31 |