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Ultiva
Ultiva - 67457-198-05 - (Remifentanil Hydrochloride)
Drug Information of Ultiva
| Product NDC: | 67457-198 |
| Proprietary Name: | Ultiva |
| Non Proprietary Name: | Remifentanil Hydrochloride |
| Active Ingredient(s): | 1 mg/mL & nbsp; Remifentanil Hydrochloride |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Ultiva
| Product NDC: | 67457-198 |
| Labeler Name: | Mylan Institutional LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA020630 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19960712 |
Package Information of Ultiva
| Package NDC: | 67457-198-05 |
| Package Description: | 10 VIAL, GLASS in 1 CARTON (67457-198-05) > 5 mL in 1 VIAL, GLASS (67457-198-99) |
NDC Information of Ultiva
| NDC Code | 67457-198-05 |
| Proprietary Name | Ultiva |
| Package Description | 10 VIAL, GLASS in 1 CARTON (67457-198-05) > 5 mL in 1 VIAL, GLASS (67457-198-99) |
| Product NDC | 67457-198 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Remifentanil Hydrochloride |
| Dosage Form Name | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 19960712 |
| Marketing Category Name | NDA |
| Labeler Name | Mylan Institutional LLC |
| Substance Name | REMIFENTANIL HYDROCHLORIDE |
| Strength Number | 1 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Full Opioid Agonists [MoA],Opioid Agonist [EPC] |
