| NDC Code | 67457-914-05 |
|---|
| Package Description | 10 VIAL, GLASS in 1 CARTON (67457-914-05) / 10 mL in 1 VIAL, GLASS (67457-914-00) |
|---|
| Product NDC | 67457-914 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Ultiva |
|---|
| Non-Proprietary Name | Remifentanil Hydrochloride |
|---|
| Dosage Form | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
|---|
| Usage | INTRAVENOUS |
|---|
| Start Marketing Date | 20200415 |
|---|
| Marketing Category Name | NDA |
|---|
| Application Number | NDA020630 |
|---|
| Manufacturer | Mylan Institutional LLC |
|---|
| Substance Name | REMIFENTANIL HYDROCHLORIDE |
|---|
| Strength | 1 |
|---|
| Strength Unit | mg/mL |
|---|
| Pharmacy Classes | Full Opioid Agonists [MoA], Opioid Agonist [EPC] |
|---|
| DEA Schedule | CII |
|---|