NDC 0406-0357 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 0406-0357 |
Marketing Category | / |
Marketing Category | ANDA |
Application Number | ANDA089160 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2010-04-22 |
Marketing End Date | 2017-09-30 |
Marketing Category | ANDA |
Application Number | ANDA089160 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2010-04-22 |
Marketing End Date | 2017-09-30 |
Marketing Category | ANDA |
Application Number | ANDA089160 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2010-02-09 |
Marketing End Date | 2017-09-30 |
Marketing Category | ANDA |
Application Number | ANDA089160 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2012-11-14 |
Marketing End Date | 2016-04-20 |
Marketing Category | ANDA |
Application Number | ANDA089160 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2010-04-22 |
Marketing End Date | 2017-09-30 |
Marketing Category | ANDA |
Application Number | ANDA089160 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2013-09-16 |
Marketing End Date | 2017-09-30 |