NDC 0093-1015 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 0093-1015 |
Marketing Category | / |
Marketing Category | ANDA |
Application Number | ANDA075189 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2001-08-20 |
Marketing End Date | 2018-06-30 |
Marketing Category | ANDA |
Application Number | ANDA075189 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2010-01-20 |
Marketing End Date | 2018-06-30 |
Marketing Category | ANDA |
Application Number | ANDA075189 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2005-02-24 |
Marketing End Date | 2017-12-31 |
Marketing Category | ANDA |
Application Number | ANDA075189 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2010-10-04 |
Marketing End Date | 2013-07-31 |