NDC 0172-4280 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 0172-4280 |
Marketing Category | / |
Marketing Category | ANDA |
Application Number | ANDA073568 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2009-09-03 |
Marketing End Date | 2014-06-03 |
Marketing Category | ANDA |
Application Number | ANDA073568 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 1992-08-01 |
Marketing End Date | 2009-09-03 |
Marketing Category | ANDA |
Application Number | ANDA073568 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 1992-08-01 |
Marketing End Date | 2009-09-03 |
Marketing Category | ANDA |
Application Number | ANDA073568 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 1992-08-01 |
Marketing End Date | 2014-06-03 |
Marketing Category | ANDA |
Application Number | ANDA073568 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 1992-08-01 |
Marketing End Date | 2015-04-30 |
Marketing Category | ANDA |
Application Number | ANDA073568 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 1992-08-01 |
Marketing End Date | 2015-04-30 |