NDC 0185-0714 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 0185-0714 |
Marketing Category | / |
Marketing Category | ANDA |
Application Number | ANDA074654 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 1996-12-31 |
Marketing End Date | 2014-11-30 |
Marketing Category | ANDA |
Application Number | ANDA074654 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 1996-12-31 |
Marketing End Date | 2014-11-30 |