NDC 68462-232 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 68462-232 |
Marketing Category | / |
Marketing Category | ANDA |
Application Number | ANDA091672 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2014-10-31 |
Marketing End Date | 2018-07-01 |
Marketing Category | ANDA |
Application Number | ANDA091672 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2014-10-31 |
Marketing End Date | 2018-07-01 |
Marketing Category | ANDA |
Application Number | ANDA091672 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2014-10-31 |
Marketing End Date | 2018-08-01 |
Marketing Category | ANDA |
Application Number | ANDA091672 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2014-10-31 |
Marketing End Date | 2018-07-01 |