NDC 0603-6151 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 0603-6151 |
Marketing Category | / |
Marketing Category | ANDA |
Application Number | ANDA090027 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2010-08-04 |
Marketing End Date | 2014-06-12 |
Marketing Category | ANDA |
Application Number | ANDA090027 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2010-08-04 |
Marketing End Date | 2016-03-31 |
Marketing Category | ANDA |
Application Number | ANDA090027 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2010-08-04 |
Marketing End Date | 2014-06-12 |
Marketing Category | ANDA |
Application Number | ANDA090027 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2010-08-04 |
Marketing End Date | 2016-03-31 |