NDC 0054-0434 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 0054-0434 |
Marketing Category | / |
Marketing Category | NDA authorized generic |
Application Number | NDA012836 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2012-02-15 |
Marketing End Date | 2018-07-31 |