NDC 63629-6803 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 63629-6803 |
Marketing Category | / |
Marketing Category | ANDA |
Application Number | ANDA078619 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2015-09-30 |
Marketing End Date | 2017-04-30 |