NDC 59762-3327 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 59762-3327 |
| Marketing Category | / |
| Marketing Category | NDA AUTHORIZED GENERIC |
| Application Number | NDA011153 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 1957-10-24 |
| Marketing End Date | 2007-05-15 |
| Marketing Category | NDA AUTHORIZED GENERIC |
| Application Number | NDA011153 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 1957-10-24 |
| Marketing End Date | 2007-05-15 |