NDC 67296-0105 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 67296-0105 |
Marketing Category | / |
Marketing Category | ANDA |
Application Number | ANDA075738 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2009-06-08 |
Inactivation Date | 2019-10-29 |