NDC 16590-234 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 16590-234 |
Marketing Category | / |
Marketing Category | ANDA |
Application Number | ANDA086414 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | GM |
Marketing Start Date | 1981-04-09 |
Inactivation Date | 2019-10-29 |
Marketing Category | ANDA |
Application Number | ANDA086414 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | GM |
Marketing Start Date | 1981-04-09 |
Inactivation Date | 2019-10-29 |
Marketing Category | ANDA |
Application Number | ANDA086414 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 1981-04-09 |
Inactivation Date | 2019-10-29 |