NDC 23155-062 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 23155-062 |
Marketing Category | / |
Marketing Category | ANDA |
Application Number | ANDA090430 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2010-11-01 |
Marketing End Date | 2018-01-10 |
Marketing Category | ANDA |
Application Number | ANDA090430 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2010-11-01 |
Marketing End Date | 2018-01-10 |
Marketing Category | ANDA |
Application Number | ANDA090430 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2010-11-01 |
Marketing End Date | 2018-01-10 |
Marketing Category | ANDA |
Application Number | ANDA090430 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2010-11-01 |
Marketing End Date | 2018-01-10 |