NDC 68084-890 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 68084-890 |
Marketing Category | / |
Marketing Category | NDA authorized generic |
Application Number | NDA021121 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2016-05-12 |
Marketing End Date | 2017-10-31 |
Marketing Category | NDA authorized generic |
Application Number | NDA021121 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2016-05-12 |
Marketing End Date | 2017-10-31 |