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 |