NDC 0172-2416 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 0172-2416 |
Marketing Category | / |
Marketing Category | ANDA |
Application Number | ANDA060704 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2000-01-31 |
Marketing End Date | 2014-11-30 |
Marketing Category | ANDA |
Application Number | ANDA060704 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2000-01-31 |
Marketing End Date | 2014-04-30 |
Marketing Category | ANDA |
Application Number | ANDA060704 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2000-01-31 |
Marketing End Date | 2014-11-30 |
Marketing Category | ANDA |
Application Number | ANDA060704 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2009-09-15 |
Marketing End Date | 2013-03-31 |