NDC 49884-235 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 49884-235 |
Marketing Category | / |
Marketing Category | ANDA |
Application Number | ANDA091632 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | ML |
Marketing Start Date | 2012-08-16 |
Marketing End Date | 2017-10-17 |
Marketing Category | ANDA |
Application Number | ANDA091632 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | ML |
Marketing Start Date | 2012-08-16 |
Marketing End Date | 2017-10-17 |