NDC 0172-4365 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 0172-4365 |
Marketing Category | / |
Marketing Category | ANDA |
Application Number | ANDA074787 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 1998-08-03 |
Marketing End Date | 2014-01-17 |
Marketing Category | ANDA |
Application Number | ANDA074787 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 1998-08-03 |
Marketing End Date | 2017-04-30 |
Marketing Category | ANDA |
Application Number | ANDA074787 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 1998-08-03 |
Marketing End Date | 2014-01-17 |
Marketing Category | ANDA |
Application Number | ANDA074787 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 1998-08-03 |
Marketing End Date | 2016-10-31 |