NDC 63629-7609 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 63629-7609 |
Marketing Category | / |
Marketing Category | ANDA |
Application Number | ANDA065248 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2018-05-25 |
Marketing End Date | 2018-05-27 |