NDC 50111-851 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 50111-851 |
Marketing Category | / |
Marketing Category | ANDA |
Application Number | ANDA081297 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 1993-04-01 |
Marketing End Date | 2015-08-31 |
Marketing Category | ANDA |
Application Number | ANDA081297 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 1993-04-01 |
Marketing End Date | 2015-08-31 |