NDC 16590-232 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 16590-232 |
Marketing Category | / |
Marketing Category | ANDA |
Application Number | ANDA071524 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 1987-12-11 |
Inactivation Date | 2019-10-29 |
Marketing Category | ANDA |
Application Number | ANDA071524 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 1987-12-11 |
Inactivation Date | 2019-10-29 |
Marketing Category | ANDA |
Application Number | ANDA071524 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 1987-12-11 |
Inactivation Date | 2019-10-29 |
Marketing Category | ANDA |
Application Number | ANDA071524 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 1987-12-11 |
Inactivation Date | 2019-10-29 |
Marketing Category | ANDA |
Application Number | ANDA071524 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 1987-12-11 |
Inactivation Date | 2019-10-29 |
Marketing Category | ANDA |
Application Number | ANDA071524 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 1987-12-11 |
Inactivation Date | 2019-10-29 |