NDC 0378-1066 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 0378-1066 |
Marketing Category | / |
Marketing Category | ANDA |
Application Number | ANDA077923 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2006-07-19 |
Marketing End Date | 2016-11-08 |
Marketing Category | ANDA |
Application Number | ANDA077923 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2006-07-19 |
Marketing End Date | 2016-11-08 |