NDC 24208-961 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 24208-961 |
Marketing Category | / |
Marketing Category | ANDA |
Application Number | ANDA074443 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | ML |
Marketing Start Date | 1995-01-30 |
Marketing End Date | 2018-06-30 |