NDC 35356-668 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 35356-668 |
Marketing Category | / |
Marketing Category | ANDA |
Application Number | ANDA077397 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2007-12-18 |
Marketing End Date | 2018-12-31 |
Marketing Category | ANDA |
Application Number | ANDA077397 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2007-12-18 |
Marketing End Date | 2016-12-31 |
Marketing Category | ANDA |
Application Number | ANDA077397 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2014-01-03 |
Marketing End Date | 2018-12-12 |