NDC 50111-394 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 50111-394 |
Marketing Category | / |
Marketing Category | ANDA |
Application Number | ANDA089059 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 1990-09-30 |
Marketing End Date | 2016-08-31 |
Marketing Category | ANDA |
Application Number | ANDA089059 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 1990-09-30 |
Marketing End Date | 2016-08-31 |