NDC 63739-455 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 63739-455 |
Marketing Category | / |
Marketing Category | ANDA |
Application Number | ANDA089160 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2010-10-25 |
Inactivation Date | 2019-10-29 |
Marketing Category | ANDA |
Application Number | ANDA089160 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2010-07-29 |
Inactivation Date | 2019-10-29 |