NDC 64376-632 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 64376-632 |
Marketing Category | / |
Marketing Category | ANDA |
Application Number | ANDA090248 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2010-10-15 |
Marketing End Date | 2017-02-28 |
Marketing Category | ANDA |
Application Number | ANDA090248 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2010-10-15 |
Marketing End Date | 2017-02-28 |
Marketing Category | ANDA |
Application Number | ANDA090248 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2010-10-15 |
Marketing End Date | 2017-02-28 |