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REMIFENTANIL HYDROCHLORIDE

NDC 0143-9391 · HUMAN PRESCRIPTION DRUG · INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION

Labeler / ManufacturerHikma Pharmaceuticals USA Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA210594
Dosage form / routeINJECTION, POWDER, LYOPHILIZED, FOR SOLUTION · INTRAVENOUS
Active ingredientsREMIFENTANIL HYDROCHLORIDE (1 mg/mL)
Marketing started20210515
Package count1

External sources

Source: openFDA. Public-domain (CC0).