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Ultiva

NDC 72078-034 · HUMAN PRESCRIPTION DRUG · INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION

Generic nameRemifentanil Hydrochloride
Labeler / ManufacturerMylan Institutional LLC
Marketing categoryNew Drug Application (innovator) · App NDA020630
Dosage form / routeINJECTION, POWDER, LYOPHILIZED, FOR SOLUTION · INTRAVENOUS
Active ingredientsREMIFENTANIL HYDROCHLORIDE (1 mg/mL)
Marketing started20230621
Package count1

External sources

Source: openFDA. Public-domain (CC0).