NDC 0037-3520 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 0037-3520 |
Marketing Category | / |
Marketing Category | NDA |
Application Number | NDA020136 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2015-01-01 |
Marketing End Date | 2018-11-30 |