NDC 76218-1828 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 76218-1828 |
Marketing Category | / |
Marketing Category | ANDA |
Application Number | ANDA040846 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2012-05-17 |
Marketing End Date | 2014-12-15 |
Marketing Category | ANDA |
Application Number | ANDA040846 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2013-09-18 |
Marketing End Date | 2014-12-15 |