NDC 0603-4248 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 0603-4248 |
Marketing Category | / |
Marketing Category | ANDA |
Application Number | ANDA077754 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2006-05-10 |
Marketing End Date | 2018-05-31 |
Marketing Category | ANDA |
Application Number | ANDA077754 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2006-05-10 |
Marketing End Date | 2018-05-31 |
Marketing Category | ANDA |
Application Number | ANDA077754 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2006-05-10 |
Marketing End Date | 2013-04-17 |
Marketing Category | ANDA |
Application Number | ANDA077754 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2006-05-10 |
Marketing End Date | 2018-05-31 |