NDC 42291-392 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 42291-392 |
Marketing Category | / |
Marketing Category | ANDA |
Application Number | ANDA076262 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2013-06-18 |
Marketing End Date | 2018-11-19 |
Marketing Category | ANDA |
Application Number | ANDA076262 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2013-06-18 |
Marketing End Date | 2018-11-19 |
Marketing Category | ANDA |
Application Number | ANDA076262 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2013-10-28 |
Marketing End Date | 2015-02-24 |