NDC 67296-0528 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 67296-0528 |
Marketing Category | / |
Marketing Category | ANDA |
Application Number | ANDA080043 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 1970-11-25 |
Inactivation Date | 2019-10-29 |