NDC 50816-624 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 50816-624 |
Marketing Category | / |
Marketing Category | NDA |
Application Number | NDA020629 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | GM |
Marketing Start Date | 2010-12-29 |
Marketing End Date | 2018-01-31 |
Marketing Category | NDA |
Application Number | NDA020629 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | GM |
Marketing Start Date | 2010-12-29 |
Marketing End Date | 2018-01-31 |