NDC 59762-5021 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 59762-5021 |
| Marketing Category | / |
| Marketing Category | NDA AUTHORIZED GENERIC |
| Application Number | NDA019885 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 1991-11-19 |
| Marketing End Date | 2018-05-31 |