NDC 49884-832 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 49884-832 |
Marketing Category | / |
Marketing Category | ANDA |
Application Number | ANDA074984 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 1999-12-24 |
Marketing End Date | 2017-11-30 |
Marketing Category | ANDA |
Application Number | ANDA074984 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 1999-12-24 |
Marketing End Date | 2018-09-30 |
Marketing Category | ANDA |
Application Number | ANDA074984 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 1999-12-24 |
Marketing End Date | 2018-09-30 |