NDC 0228-2717 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 0228-2717 |
Marketing Category | / |
Marketing Category | ANDA |
Application Number | ANDA075910 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2002-01-09 |
Marketing End Date | 2016-09-30 |