NDC 49999-631 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 49999-631 |
Marketing Category | / |
Marketing Category | ANDA |
Application Number | ANDA077584 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2007-04-13 |
Marketing End Date | 2018-10-11 |
Marketing Category | ANDA |
Application Number | ANDA077584 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2007-04-13 |
Marketing End Date | 2018-10-11 |