NDC 53746-113 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 53746-113 |
Marketing Category | / |
Marketing Category | ANDA |
Application Number | ANDA040754 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2010-02-18 |
Marketing End Date | 2014-04-01 |
Marketing Category | ANDA |
Application Number | ANDA040754 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2010-02-18 |
Marketing End Date | 2014-04-01 |