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 |