NDC 67767-151 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 67767-151 |
Marketing Category | / |
Marketing Category | ANDA |
Application Number | ANDA077899 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2007-06-22 |
Marketing End Date | 2014-07-31 |
Marketing Category | ANDA |
Application Number | ANDA077899 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2007-06-22 |
Marketing End Date | 2014-07-31 |