NDC 0603-3856 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 0603-3856 |
Marketing Category | / |
Marketing Category | ANDA |
Application Number | ANDA040412 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2002-03-29 |
Marketing End Date | 2018-09-26 |
Marketing Category | ANDA |
Application Number | ANDA040412 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2002-03-29 |
Marketing End Date | 2018-09-26 |
Marketing Category | ANDA |
Application Number | ANDA040412 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2002-03-29 |
Marketing End Date | 2018-09-26 |
Marketing Category | ANDA |
Application Number | ANDA040412 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2002-03-29 |
Marketing End Date | 2018-09-26 |
Marketing Category | ANDA |
Application Number | ANDA040412 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2002-03-29 |
Marketing End Date | 2018-09-26 |
Marketing Category | ANDA |
Application Number | ANDA040412 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2002-03-29 |
Marketing End Date | 2018-09-26 |
Marketing Category | ANDA |
Application Number | ANDA040412 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2002-03-29 |
Marketing End Date | 2018-09-26 |