NDC 64950-322 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 64950-322 |
Marketing Category | / |
Marketing Category | NDA |
Application Number | NDA206814 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | ML |
Marketing Start Date | 2015-02-15 |
Marketing End Date | 2015-09-07 |