NDC 0172-3626 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 0172-3626 |
Marketing Category | / |
Marketing Category | ANDA |
Application Number | ANDA062505 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2011-02-10 |
Marketing End Date | 2013-09-05 |
Marketing Category | ANDA |
Application Number | ANDA062505 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 1984-09-11 |
Marketing End Date | 2014-07-31 |
Marketing Category | ANDA |
Application Number | ANDA062505 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 1984-09-11 |
Marketing End Date | 2014-07-31 |
Marketing Category | ANDA |
Application Number | ANDA062505 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2011-02-10 |
Marketing End Date | 2013-09-05 |