NDC 0062-0165 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 0062-0165 |
Marketing Category | / |
Marketing Category | NDA |
Application Number | NDA019049 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | GM |
Marketing Start Date | 1988-10-30 |
Marketing End Date | 2016-09-30 |
Marketing Category | NDA |
Application Number | NDA019049 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | GM |
Marketing Start Date | 1988-10-30 |
Marketing End Date | 2015-08-31 |