NDC 16252-529 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 16252-529 |
Marketing Category | / |
Marketing Category | ANDA |
Application Number | ANDA076939 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2017-12-28 |
Marketing End Date | 2018-07-31 |
Marketing Category | ANDA |
Application Number | ANDA076939 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2012-02-16 |
Marketing End Date | 2015-11-06 |
Marketing Category | ANDA |
Application Number | ANDA076939 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2007-12-28 |
Marketing End Date | 2015-11-06 |
Marketing Category | ANDA |
Application Number | ANDA076939 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2007-12-28 |
Marketing End Date | 2018-06-30 |