NDC 60505-2782 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 60505-2782 |
Marketing Category | / |
Marketing Category | ANDA |
Application Number | ANDA078777 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2012-09-11 |
Marketing End Date | 2016-08-07 |
Marketing Category | ANDA |
Application Number | ANDA078777 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2012-09-11 |
Marketing End Date | 2016-08-07 |
Marketing Category | ANDA |
Application Number | ANDA078777 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2012-09-11 |
Marketing End Date | 2016-08-07 |
Marketing Category | ANDA |
Application Number | ANDA078777 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2012-09-11 |
Marketing End Date | 2016-08-07 |