NDC 51079-557 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 51079-557 |
Marketing Category | / |
Marketing Category | ANDA |
Application Number | ANDA077665 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2012-05-17 |
Marketing End Date | 2018-11-30 |
Marketing Category | ANDA |
Application Number | ANDA077665 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2012-05-17 |
Marketing End Date | 2018-11-30 |