NDC 47335-175 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 47335-175 |
Marketing Category | / |
Marketing Category | ANDA |
Application Number | ANDA090362 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2013-02-05 |
Marketing End Date | 2017-10-31 |
Marketing Category | ANDA |
Application Number | ANDA090362 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2013-02-05 |
Marketing End Date | 2017-10-31 |
Marketing Category | ANDA |
Application Number | ANDA090362 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2013-02-05 |
Marketing End Date | 2017-10-31 |
Marketing Category | ANDA |
Application Number | ANDA090362 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2013-02-05 |
Marketing End Date | 2017-10-31 |
Marketing Category | ANDA |
Application Number | ANDA090362 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2013-02-05 |
Marketing End Date | 2017-10-31 |