NDC 53489-433 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 53489-433 |
Marketing Category | / |
Marketing Category | ANDA |
Application Number | ANDA040525 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2003-10-23 |
Marketing End Date | 2019-01-31 |
Marketing Category | ANDA |
Application Number | ANDA040525 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2003-10-23 |
Marketing End Date | 2019-01-31 |
Marketing Category | ANDA |
Application Number | ANDA040525 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2003-10-23 |
Marketing End Date | 2019-01-31 |
Marketing Category | ANDA |
Application Number | ANDA040525 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2003-10-23 |
Marketing End Date | 2019-01-31 |
Marketing Category | ANDA |
Application Number | ANDA040525 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2003-10-23 |
Marketing End Date | 2019-01-31 |
Marketing Category | ANDA |
Application Number | ANDA040525 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2003-10-23 |
Marketing End Date | 2019-01-31 |