NDC 0172-3649 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 0172-3649 |
Marketing Category | / |
Marketing Category | ANDA |
Application Number | ANDA074497 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2009-06-09 |
Marketing End Date | 2014-01-31 |
Marketing Category | ANDA |
Application Number | ANDA074497 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 1995-09-12 |
Marketing End Date | 2015-10-31 |
Marketing Category | ANDA |
Application Number | ANDA074497 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 1995-09-12 |
Marketing End Date | 2009-07-31 |
Marketing Category | ANDA |
Application Number | ANDA074497 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 1995-09-12 |
Marketing End Date | 2015-10-31 |