NDC 50111-563 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 50111-563 |
Marketing Category | / |
Marketing Category | ANDA |
Application Number | ANDA074421 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 1995-09-29 |
Marketing End Date | 2016-10-31 |
Marketing Category | ANDA |
Application Number | ANDA074421 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 1995-09-29 |
Marketing End Date | 2016-10-31 |
Marketing Category | ANDA |
Application Number | ANDA074421 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 1995-09-29 |
Marketing End Date | 2016-10-31 |