NDC 16781-457 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 16781-457 |
Marketing Category | / |
Marketing Category | NDA |
Application Number | NDA050649 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 1999-05-31 |
Marketing End Date | 2017-05-18 |
Marketing Category | NDA |
Application Number | NDA050649 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 1999-05-31 |
Marketing End Date | 2017-05-18 |