NDC 67253-389 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 67253-389 |
Marketing Category | / |
Marketing Category | ANDA |
Application Number | ANDA062500 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 1984-09-11 |
Marketing End Date | 2018-03-31 |
Marketing Category | ANDA |
Application Number | ANDA062500 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 1984-09-11 |
Marketing End Date | 2019-01-31 |