NDC 0603-2957 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 0603-2957 |
Marketing Category | / |
Marketing Category | ANDA |
Application Number | ANDA077901 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2007-03-09 |
Marketing End Date | 2018-09-23 |
Marketing Category | ANDA |
Application Number | ANDA077901 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2007-03-09 |
Marketing End Date | 2018-09-23 |
Marketing Category | ANDA |
Application Number | ANDA077901 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2007-03-09 |
Marketing End Date | 2018-09-23 |
Marketing Category | ANDA |
Application Number | ANDA077901 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2007-03-09 |
Marketing End Date | 2018-09-23 |
Marketing Category | ANDA |
Application Number | ANDA077901 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2007-03-09 |
Marketing End Date | 2018-09-23 |
Marketing Category | ANDA |
Application Number | ANDA077901 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2007-03-09 |
Marketing End Date | 2018-09-23 |
Marketing Category | ANDA |
Application Number | ANDA077901 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2007-03-09 |
Marketing End Date | 2018-09-23 |