NDC 53808-0734 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 53808-0734 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA071839 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2009-07-01 |
| Inactivation Date | 2020-01-31 |