NDC 69543-142 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 69543-142 |
Marketing Category | / |
Marketing Category | ANDA |
Application Number | ANDA090382 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2015-07-14 |
Marketing End Date | 2018-10-31 |
Marketing Category | ANDA |
Application Number | ANDA090382 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2015-07-14 |
Marketing End Date | 2015-07-14 |
Marketing Category | ANDA |
Application Number | ANDA090382 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2015-07-14 |
Marketing End Date | 2018-11-30 |
Marketing Category | ANDA |
Application Number | ANDA090382 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2015-07-14 |
Marketing End Date | 2018-10-31 |