NDC 50111-393 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 50111-393 |
Marketing Category | / |
Marketing Category | ANDA |
Application Number | ANDA089058 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 1990-09-30 |
Marketing End Date | 2017-02-28 |
Marketing Category | ANDA |
Application Number | ANDA089058 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 1990-09-30 |
Marketing End Date | 2013-10-02 |