NDC 61894-002 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 61894-002 |
Marketing Category | / |
Marketing Category | NDA |
Application Number | NDA020184 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2014-10-10 |
Marketing End Date | 2014-11-18 |
Marketing Category | NDA |
Application Number | NDA020184 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2014-10-10 |
Marketing End Date | 2017-03-01 |