NDC 60505-2582 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 60505-2582 |
Marketing Category | / |
Marketing Category | ANDA |
Application Number | ANDA065509 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2018-11-15 |
Marketing End Date | 2018-11-16 |
Marketing Category | ANDA |
Application Number | ANDA065509 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2018-11-15 |
Marketing End Date | 2014-08-25 |
Marketing Category | ANDA |
Application Number | ANDA065509 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2018-11-15 |
Marketing End Date | 2018-11-16 |
Marketing Category | ANDA |
Application Number | ANDA065509 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2018-11-15 |
Marketing End Date | 2018-11-16 |