NDC 0172-3761 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 0172-3761 |
Marketing Category | / |
Marketing Category | ANDA |
Application Number | ANDA075752 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2002-07-01 |
Marketing End Date | 2017-03-31 |
Marketing Category | ANDA |
Application Number | ANDA075752 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2002-07-01 |
Marketing End Date | 2017-03-31 |
Marketing Category | ANDA |
Application Number | ANDA075752 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2002-07-01 |
Marketing End Date | 2013-12-31 |
Marketing Category | ANDA |
Application Number | ANDA075752 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2002-07-01 |
Marketing End Date | 2017-03-31 |