NDC 59630-912 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 59630-912 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA040658 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2011-10-10 |
| Marketing End Date | 2018-01-22 |