NDC 47335-604 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 47335-604 |
Marketing Category | / |
Marketing Category | ANDA |
Application Number | ANDA090082 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2010-06-18 |
Marketing End Date | 2016-11-30 |
Marketing Category | ANDA |
Application Number | ANDA090082 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2010-06-18 |
Marketing End Date | 2016-11-30 |
Marketing Category | ANDA |
Application Number | ANDA090082 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2010-06-18 |
Marketing End Date | 2016-11-30 |
Marketing Category | ANDA |
Application Number | ANDA090082 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2010-06-18 |
Marketing End Date | 2016-11-30 |
Marketing Category | ANDA |
Application Number | ANDA090082 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2010-06-18 |
Marketing End Date | 2016-11-30 |