NDC 49884-685 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 49884-685 |
Marketing Category | / |
Marketing Category | ANDA |
Application Number | ANDA070581 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 1985-10-17 |
Marketing End Date | 2019-01-23 |
Marketing Category | ANDA |
Application Number | ANDA070581 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 1985-10-17 |
Marketing End Date | 2019-01-23 |