NDC 63304-657 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 63304-657 |
Marketing Category | / |
Marketing Category | ANDA |
Application Number | ANDA065007 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 1998-07-28 |
Marketing End Date | 2011-08-29 |
Marketing Category | ANDA |
Application Number | ANDA065007 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 1998-07-28 |
Marketing End Date | 2011-08-29 |
Marketing Category | ANDA |
Application Number | ANDA065007 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 1998-07-28 |
Marketing End Date | 2011-08-29 |