NDC 16252-572 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 16252-572 |
Marketing Category | / |
Marketing Category | ANDA |
Application Number | ANDA076549 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2007-12-26 |
Marketing End Date | 2018-12-31 |
Marketing Category | ANDA |
Application Number | ANDA076549 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2007-12-26 |
Marketing End Date | 2018-12-31 |