NDC 16590-284 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 16590-284 |
Marketing Category | / |
Marketing Category | ANDA |
Application Number | ANDA077293 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2006-02-01 |
Inactivation Date | 2019-11-13 |
Marketing Category | ANDA |
Application Number | ANDA077293 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2006-02-01 |
Inactivation Date | 2019-11-13 |
Marketing Category | ANDA |
Application Number | ANDA077293 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2006-02-01 |
Inactivation Date | 2019-11-13 |
Marketing Category | ANDA |
Application Number | ANDA077293 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2006-02-01 |
Inactivation Date | 2019-11-13 |