NDC 60429-791 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 60429-791 |
Marketing Category | / |
Marketing Category | ANDA |
Application Number | ANDA040301 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 1999-07-15 |
Marketing End Date | 2016-04-30 |
Marketing Category | ANDA |
Application Number | ANDA040301 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 1999-07-15 |
Marketing End Date | 2014-04-30 |
Marketing Category | ANDA |
Application Number | ANDA040301 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 1999-07-15 |
Marketing End Date | 2015-02-28 |
Marketing Category | ANDA |
Application Number | ANDA040301 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 1999-07-15 |
Marketing End Date | 2017-11-30 |
Marketing Category | ANDA |
Application Number | ANDA040301 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 1999-07-15 |
Marketing End Date | 2017-11-30 |