NDC 62756-755 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 62756-755 |
Marketing Category | / |
Marketing Category | ANDA |
Application Number | ANDA090881 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2012-02-28 |
Marketing End Date | 2018-05-31 |
Marketing Category | ANDA |
Application Number | ANDA090881 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2012-02-28 |
Marketing End Date | 2018-05-31 |