Is Tubocurarine registered with the SFDA?

The SFDA human drug list (edition 4-2026, as published by the Council of Health Insurance) lists 0 valid registrations of Tubocurarine.

Is Tubocurarine approved by the US FDA?

Drugs@FDA lists 4 application product lines for Tubocurarine, including TUBOCURARINE CHLORIDE (Discontinued); TUBOCURARINE CHLORIDE (Discontinued); TUBOCURARINE CHLORIDE (Discontinued); TUBOCURARINE CHLORIDE (Discontinued).

Active substance

Tubocurarine

SFDA 1
US FDA 4

Open in the medicines table

SFDA Saudi Arabia — SFDA human drug list

Trade name	Strength	Form · route	Pack	Public price	Type	Company	Status
TUBOCURARINE HYDROCHLORIDE INJ F.T.V.	3 mg/ml	Injection · Intravenous use	1 Vial	SAR 35.70	NCE · Prescription	HOSPIRA INC	Withdrawn by MAH · Not Marketed

US FDA United States — FDA approvals (Drugs@FDA)

Product	Strength	Form · route	Applicant	Status	First approved
TUBOCURARINE CHLORIDE	3MG/ML	injectable · injection	BRISTOL MYERS SQUIBB	Discontinued	20 Feb 1945
TUBOCURARINE CHLORIDE	3MG/ML	injectable · injection	HOSPIRA	Discontinued	30 Jan 1947
TUBOCURARINE CHLORIDE	3MG/ML	injectable · injection	LILLY	Discontinued	28 Nov 1947
TUBOCURARINE CHLORIDE	3MG/ML	injectable · injection	QUAD PHARMS	Discontinued

Values as published by each source: SFDA human drug list (4-2026, as published by the Council of Health Insurance; indications from the CHI Daman Drug Formulary), Drugs@FDA, EMA medicines data, Health Canada Drug Product Database (Open Government Licence – Canada), CMS NADAC, NHS Drug Tariff Part VIIIA (NHSBSA Copyright, Open Government Licence v3.0), WHO Model List of Essential Medicines (CC BY 3.0 IGO; regrouped by active substance, not created by WHO), EMA PRAC, US FDA safety-related labeling changes and MHRA Drug Safety Update (Open Government Licence v3.0). Sources and reuse. Not a substitute for the official registers or the product information.