NDC 0378-1053 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 0378-1053 |
Marketing Category | / |
Marketing Category | ANDA |
Application Number | ANDA075480 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2000-08-22 |
Marketing End Date | 2019-01-31 |
Marketing Category | ANDA |
Application Number | ANDA075480 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2000-08-22 |
Marketing End Date | 2019-01-31 |