NDC 0093-4030 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 0093-4030 |
Marketing Category | / |
Marketing Category | ANDA |
Application Number | ANDA070756 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2007-12-14 |
Marketing End Date | 2014-04-09 |
Marketing Category | ANDA |
Application Number | ANDA070756 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2007-12-14 |
Marketing End Date | 2018-04-30 |
Marketing Category | ANDA |
Application Number | ANDA070756 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2007-12-14 |
Marketing End Date | 2014-04-09 |
Marketing Category | ANDA |
Application Number | ANDA070756 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2007-12-14 |
Marketing End Date | 2018-04-30 |