NDC 35781-0500 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 35781-0500 |
| Marketing Category | / |
| Marketing Category | Premarket Notification |
| Application Number | K092086 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | ML |
| Marketing Start Date | 2009-06-30 |
| Inactivation Date | 2020-01-31 |
| Marketing Category | Premarket Notification |
| Application Number | K092086 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2009-06-30 |
| Inactivation Date | 2020-01-31 |
| Marketing Category | Premarket Notification |
| Application Number | K092086 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2009-06-30 |
| Inactivation Date | 2020-01-31 |