NDC 68001-230 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 68001-230 |
Marketing Category | / |
Marketing Category | ANDA |
Application Number | ANDA070044 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2014-03-13 |
Marketing End Date | 2015-12-31 |