NDC 49884-407 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 49884-407 |
Marketing Category | / |
Marketing Category | NDA authorized generic |
Application Number | NDA019962 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2007-07-26 |
Marketing End Date | 2016-11-30 |
Marketing Category | NDA authorized generic |
Application Number | NDA019962 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2007-07-26 |
Marketing End Date | 2016-11-30 |