NDC 76439-134 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 76439-134 |
Marketing Category | / |
Marketing Category | ANDA |
Application Number | ANDA200958 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2013-12-15 |
Marketing End Date | 2016-05-05 |
Marketing Category | ANDA |
Application Number | ANDA200958 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2013-12-15 |
Marketing End Date | 2016-05-05 |