NDC 0093-4356 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 0093-4356 |
Marketing Category | / |
Marketing Category | ANDA |
Application Number | ANDA075245 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2008-11-06 |
Marketing End Date | 2012-04-10 |
Marketing Category | ANDA |
Application Number | ANDA075245 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2008-11-06 |
Marketing End Date | 2014-03-31 |
Marketing Category | ANDA |
Application Number | ANDA075245 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2008-11-06 |
Marketing End Date | 2012-04-10 |
Marketing Category | ANDA |
Application Number | ANDA075245 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2008-11-06 |
Marketing End Date | 2014-03-31 |
Marketing Category | ANDA |
Application Number | ANDA075245 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2008-11-06 |
Marketing End Date | 2012-04-10 |