NDC 66657-301 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 66657-301 |
| Marketing Category | / |
| Marketing Category | NDA |
| Application Number | NDA019961 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | ML |
| Marketing Start Date | 2003-09-17 |
| Marketing Category | NDA |
| Application Number | NDA019961 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | ML |
| Marketing Start Date | 2003-09-17 |
| Inactivation Date | 2019-11-13 |