NDC 24658-250 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 24658-250 |
Marketing Category | / |
Marketing Category | ANDA |
Application Number | ANDA076558 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2009-08-11 |
Marketing End Date | 2017-06-30 |
Marketing Category | ANDA |
Application Number | ANDA076558 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2009-08-11 |
Marketing End Date | 2017-06-30 |
Marketing Category | ANDA |
Application Number | ANDA076558 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2009-08-11 |
Marketing End Date | 2017-06-30 |
Marketing Category | ANDA |
Application Number | ANDA076558 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2009-08-11 |
Marketing End Date | 2017-06-30 |
Marketing Category | ANDA |
Application Number | ANDA076558 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2009-08-11 |
Marketing End Date | 2017-06-30 |
Marketing Category | ANDA |
Application Number | ANDA076558 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2009-08-11 |
Marketing End Date | 2017-06-30 |