NDC 62037-720 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 62037-720 |
Marketing Category | / |
Marketing Category | ANDA |
Application Number | ANDA075604 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2002-04-10 |
Marketing End Date | 2017-05-31 |
Marketing Category | ANDA |
Application Number | ANDA075604 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2002-04-10 |
Marketing End Date | 2015-01-31 |
Marketing Category | ANDA |
Application Number | ANDA075604 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2002-04-10 |
Marketing End Date | 2017-08-31 |