NDC 60505-3779 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 60505-3779 |
Marketing Category | / |
Marketing Category | NDA AUTHORIZED GENERIC |
Application Number | NDA020699 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2011-06-10 |
Marketing End Date | 2015-11-01 |
Marketing Category | NDA AUTHORIZED GENERIC |
Application Number | NDA020699 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2011-06-10 |
Marketing End Date | 2015-09-01 |