NDC 35356-877 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 35356-877 |
Marketing Category | / |
Marketing Category | ANDA |
Application Number | ANDA077438 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2011-06-20 |
Marketing End Date | 2017-06-01 |
Marketing Category | ANDA |
Application Number | ANDA077438 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2011-06-20 |
Marketing End Date | 2017-06-01 |
Marketing Category | ANDA |
Application Number | ANDA077438 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2011-06-20 |
Marketing End Date | 2017-06-01 |
Marketing Category | ANDA |
Application Number | ANDA077438 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2011-06-20 |
Marketing End Date | 2017-06-01 |
Marketing Category | ANDA |
Application Number | ANDA077438 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2011-06-20 |
Marketing End Date | 2017-06-01 |