NDC 0093-1039 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 0093-1039 |
Marketing Category | / |
Marketing Category | ANDA |
Application Number | ANDA075435 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2004-10-08 |
Marketing End Date | 2010-01-20 |
Marketing Category | ANDA |
Application Number | ANDA075435 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2004-10-08 |
Marketing End Date | 2010-01-20 |
Marketing Category | ANDA |
Application Number | ANDA075435 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2008-07-11 |
Marketing End Date | 2010-08-31 |
Marketing Category | ANDA |
Application Number | ANDA075435 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2004-10-08 |
Marketing End Date | 2014-08-31 |
Marketing Category | ANDA |
Application Number | ANDA075435 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2010-01-20 |
Marketing End Date | 2014-08-31 |