NDC 0603-1393 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 0603-1393 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA040708 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | ML |
| Marketing Start Date | 2007-02-27 |
| Marketing End Date | 2018-05-31 |