NDC 62175-181 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 62175-181 |
Marketing Category | / |
Marketing Category | ANDA |
Application Number | ANDA078281 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2011-01-20 |
Marketing End Date | 2017-08-15 |
Marketing Category | ANDA |
Application Number | ANDA078281 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2011-01-20 |
Marketing End Date | 2017-08-15 |