NDC 0093-2131 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 0093-2131 |
Marketing Category | / |
Marketing Category | ANDA |
Application Number | ANDA073652 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2007-03-08 |
Marketing End Date | 2017-12-31 |
Marketing Category | ANDA |
Application Number | ANDA073652 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2007-03-08 |
Marketing End Date | 2017-12-31 |
Marketing Category | ANDA |
Application Number | ANDA073652 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2007-12-20 |
Marketing End Date | 2013-12-31 |
Marketing Category | ANDA |
Application Number | ANDA073652 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2007-03-08 |
Marketing End Date | 2017-09-30 |