NDC 52544-143 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 52544-143 |
Marketing Category | / |
Marketing Category | ANDA |
Application Number | ANDA076629 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2010-12-01 |
Marketing End Date | 2016-07-31 |