NDC 63629-6469 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 63629-6469 |
Marketing Category | / |
Marketing Category | ANDA |
Application Number | ANDA202556 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2015-11-03 |
Marketing End Date | 2017-01-30 |