NDC 0378-4070 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 0378-4070 |
Marketing Category | / |
Marketing Category | ANDA |
Application Number | ANDA074035 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 1997-01-15 |
Marketing End Date | 2016-01-31 |