NDC 49884-821 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 49884-821 |
Marketing Category | / |
Marketing Category | ANDA |
Application Number | ANDA078783 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2012-06-28 |
Marketing End Date | 2018-10-31 |
Marketing Category | ANDA |
Application Number | ANDA078783 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2012-06-28 |
Marketing End Date | 2017-06-21 |
Marketing Category | ANDA |
Application Number | ANDA078783 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2012-06-28 |
Marketing End Date | 2017-01-11 |
Marketing Category | ANDA |
Application Number | ANDA078783 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2012-06-28 |
Marketing End Date | 2011-01-06 |